Vaccines, Blood & Biologics
Resources for You
March 4, 2011
Mediware Information Systems, Inc.
Attention: Mr. James C. McGaha
1900 Spring Road, Suite 450
Oak Brook, IL 60523
|Trade/Device Name:||LifeTrak®/ Plasma, Version 1.0.0|
|Product Name:||Software, Blood Bank, Stand Alone|
|Dated:||December 17, 2010|
|Received:||December 20, 2010|
Dear Mr. McGaha:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, ″Misbranding by reference to premarket notification″ (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
for Richard J. Davey, M.D.
Division of Blood Applications
Office of Blood Research and Review
Center for Biologics
Evaluation and Research
Indications for Use
|Device Name:||LifeTrak®/ Plasma, Version 1.0.0|
Indications For Use:
LifeTrak®/Plasma is a comprehensive modular computerized system intended to be used by trained personnel as a tool in the management of data related to donors, plasma collection, processing, testing, and distribution of Source Plasma for use in the production on injectable and non-injectable plasma derived products:
- Maintaining a reliable source plasma donor database
- Rolling source plasma donor eligibility status and calculation of donor status
- On-line health history, physical findings, and donor questionnaire
- Inter-active donor questionnaire (staff and/or donor)
- Donor and product testing
- Donor notification
- Source plasma collection, processing, testing and distribution
- Printing plasma and case labels
Data generated during donor eligibility determination, plasma collection and plasma processing for multiple plasma collection centers is consolidated in an enterprise centralized database that is accessible real-time through connection with a central computer system.