![]() | ||||||||||||||||||||||||||||||||||
FDA 510(k) Applications for Medical Device Product Code "DWS"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K955689 | CONTOUR FABRICATORS OF FLORIDA, INC. | RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY | 05/15/1996 |
K964445 | DLP, INC. | OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006) | 01/30/1997 |
K960139 | GE MEDICAL SYSTEMS | G.E. STERILE ANGIOGRAPHIC TRAY | 04/19/1996 |
K960144 | GE MEDICAL SYSTEMS | G.E. STERILE CT BIOPSY TRAY | 04/15/1996 |
K960143 | GE MEDICAL SYSTEMS | G.E. STERILE DIGITAL ANGIOGRAPHIC TRAY | 04/09/1996 |
K022238 | MEDTRONIC VASCULAR | MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626 | 10/09/2002 |
K962771 | PILLING WECK, INC. | BURKE CONGENITAL THORACOSCOPY INSTRUMENTS | 11/19/1996 |