FDA 510(k) Applications Submitted by GRETCHEN Y COHEN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K970945 |
03/14/1997 |
ANGLED TIP POLYPECTOMY SNARE |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K963051 |
08/06/1996 |
ERCP CANNULA |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K040494 |
02/26/2004 |
CAPSULE DELIVERY DEVICE, 160CM, MODEL 711143; CAPSULE DELIVERY DEVICE, 210CM, MODEL 711144 |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K040836 |
03/31/2004 |
DISPOSABLE OVERTUBE |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K040961 |
04/13/2004 |
INJECTOR NEEDLE/SNARE |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K971842 |
05/19/1997 |
COAXIAL NEEDLE |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K051637 |
06/20/2005 |
DSNARE, MODEL 00711087 |
UNITED STATES ENDOSCOPY GROUP, INC. |
| K972505 |
07/03/1997 |
RESUABLE HOT BIOPSY FORCEPS |
UNITED STATES ENDOSCOPY GROUP, INC. |
|
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