The following data is part of a premarket notification filed by American V. Mueller with the FDA for V. Mueller (r) Gooseneck Circular Stapler.
| Device ID | K862772 |
| 510k Number | K862772 |
| Device Name: | V. MUELLER (R) GOOSENECK CIRCULAR STAPLER |
| Classification | Stapler, Surgical |
| Applicant | AMERICAN V. MUELLER 6600 W. TOUHY Chicago, IL 60648 |
| Contact | Matthew Nowland |
| Correspondent | Matthew Nowland AMERICAN V. MUELLER 6600 W. TOUHY Chicago, IL 60648 |
| Product Code | GAG |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-07-22 |
| Decision Date | 1986-08-18 |