The following data is part of a premarket notification filed by Vance Products, Inc. with the FDA for Vance-ambrose Resectoscope Forceps.
| Device ID | K812785 |
| 510k Number | K812785 |
| Device Name: | VANCE-AMBROSE RESECTOSCOPE FORCEPS |
| Classification | Forceps, General & Plastic Surgery |
| Applicant | VANCE PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GEN |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-05 |
| Decision Date | 1981-11-16 |