The following data is part of a premarket notification filed by United States Endoscopy Group, Inc. with the FDA for Percutaneous Replacement Gastrostomy Feeding Catheter Tray (modification).
| Device ID | K954879 |
| 510k Number | K954879 |
| Device Name: | PERCUTANEOUS REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY (MODIFICATION) |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | UNITED STATES ENDOSCOPY GROUP, INC. 9300 PROGRESS PKWY. Mentor, OH 44060 |
| Contact | Gretchen Younker |
| Correspondent | Gretchen Younker UNITED STATES ENDOSCOPY GROUP, INC. 9300 PROGRESS PKWY. Mentor, OH 44060 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-10-13 |
| Decision Date | 1996-03-29 |