The following data is part of a premarket notification filed by Minto Research & Development, Inc. with the FDA for Forceps.
| Device ID | K904723 |
| 510k Number | K904723 |
| Device Name: | FORCEPS |
| Classification | Forceps, General & Plastic Surgery |
| Applicant | MINTO RESEARCH & DEVELOPMENT, INC. 3676 CHARLANNE DR. Redding, CA 96002 |
| Contact | Robert Williams |
| Correspondent | Robert Williams MINTO RESEARCH & DEVELOPMENT, INC. 3676 CHARLANNE DR. Redding, CA 96002 |
| Product Code | GEN |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-17 |
| Decision Date | 1991-07-26 |