IMPRUV A.I. CREAM WOUND AND SKIN EMULSION
Jul 2005
425d
Stiefel Laboratories, Inc.
1
Total
1
Cleared
0
Denied
Stiefel Laboratories, Inc. has 1 FDA 510(k) cleared medical devices. Based in Oak Hill, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stiefel Laboratories, Inc. Filter by specialty or product code using the sidebar.
1 devices