FDA 510(k) Applications for Medical Device Product Code "GER"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960236 | CUSTOM PACK RELIABILITY | CPR LAP SPONGES | 03/28/1996 |
K990332 | DUMEX MEDICAL SURGICAL PRODUCTS, LTD. | DUMEX IODOFORM PACKING STRIP | 04/14/1999 |
K971473 | M-PACT WORLDWIDE MANAGEMENT CORP. | IVALON INSTRUMENT WIPE, IVALON KNIFE CLEANING BLOCK | 07/07/1997 |
K960621 | SHIPPERT MEDICAL TECHNOLOGIES CORP. | EXPANDACELL INSTRUMENT WIPE | 04/01/1996 |