The following data is part of a premarket notification filed by Edward Weck, Inc. with the FDA for Vogler Hysterectomy Forceps (small & Lg).
| Device ID | K810391 |
| 510k Number | K810391 |
| Device Name: | VOGLER HYSTERECTOMY FORCEPS (SMALL & LG) |
| Classification | Forceps, Surgical, Gynecological |
| Applicant | EDWARD WECK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HCZ |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-02-17 |
| Decision Date | 1981-03-04 |