The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar Foerster Forceps.
| Device ID | K821349 |
| 510k Number | K821349 |
| Device Name: | CONPHAR FOERSTER FORCEPS |
| Classification | Forceps, General & Plastic Surgery |
| Applicant | CONPHAR, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | GEN |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-05 |
| Decision Date | 1982-05-25 |