FDA 510(k) Applications for Medical Device Product Code "GBW"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960426 | MEDICAL COMPONENTS, INC. | MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER | 03/21/1996 |
K961194 | SIL-MED CORP. | ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN | 08/08/1996 |
K942709 | SIL-MED CORP. | MEDIASTINAL SILICONE DRAINS | 01/04/1996 |
K992907 | TAUT, INC. | INTRADUCER | 10/05/1999 |
K972112 | TAUT, INC. | INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450 | 12/01/1997 |
K992904 | TAUT, INC. | MINI-PORT | 10/05/1999 |