March 12, 1992
Donald H. Buchholz, M.D.
Baxter Healthcare Corporation
Route 120 and Wilson Road
Round Lake, IL 60073
Product: Fenwal Needle/Tube Sampling Protector and Needle Safety Cover
Date Received: 12-MAR-1992
Dear Dr. Buchholz:
The Center for Biologics Evaluation and Research has completed its review of your Premarket Notification [510(k)] of intent to market the above device and we have determined that the device is substantially equivalent to devices marketed in interstate commerce prior to enactment of the Medical Device Amendments, May 28, 1976. You may, therefore, market your device subject to the general controls provisions of the Federal Food, Drug and Cosmetic Act.
General controls presently include regulations on annual registration, listing of devices, good manufacturing practices, labeling, and the misbranding and adulteration provisions of the Act. In the near future, the scope of general controls may be broadened to include additional regulations relating to restricted devices, records and reports, and others.
This letter should not be construed as approval of your device, rather it indicates that sufficient information has been submitted to determine that the device is substantially equivalent to another device previously marketed in interstate commerce.
Gerald V. Quinnan, Jr., M.D.
Center for Biologics Evaluation and Research