FDA STAFF MANUAL GUIDES, VOLUME II - DELEGATIONS OF AUTHORITY
REGULATORY - MEDICAL DEVICES AND RADIOLOGICAL HEALTH
NOTIFICATION TO SPONSORS OF DEFICIENCIES IN PETITIONS FOR RECLASSIFICATION OF MEDICAL DEVICES
Effective Date: 03/23/2011
1. AUTHORITY DELEGATED AND TO WHOM DELEGATED.
The following officials, for medical devices assigned to their respective organizations, are authorized to notify sponsors of deficiencies in petitions for reclassification of medical devices submitted under Sections 513(f) and 520(l) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360c(f) and 360j(l)):
1. Director and Deputy Directors, Center for Devices and Radiological Health (CDRH); Director and Deputy Directors, Office of Device Evaluation (ODE), CDRH; Director, Program Operations Staff, ODE, CDRH; and Director and Deputy Directors, Office of In Vitro Diagnostic Device Evaluation and Safety, CDRH
2. Director and Deputy Director, Center for Biologics Evaluation and Research (CBER); Director and Deputy Directors, Office of Blood Research and Review, CBER; Director and Deputy Director, Office of Vaccines Research and Review, CBER; and Director and Deputy Director, Office of Cellular, Tissue and Gene Therapies, CBER
3. Director and Deputy Directors, Center for Drug Evaluation and Research, (CDER); and Director and Deputy Director, Office of New Drugs, CDER
These officials may not further redelegate this authority.
3. EFFECTIVE DATE.
The Commissioner of Food and Drugs approved this delegation, via memorandum, on March 23, 2011.
|STATUS (I, R, C)||DATE APPROVED||LOCATION OF CHANGE HISTORY||CONTACT||APPROVING OFFICIAL|
|Initial||06/23/2009||N/a||OC/OO/OM/OMP||Commissioner of Food and Drugs|
|Revision||03/23/2011||N/a||CDRH/OMO/DEMO/AMB||Margaret A. Hamburg, M.D., Commissioner of Food and Drugs|