The following data is part of a premarket notification filed by Eder Instrument Co, Inc. with the FDA for Grasping Forcep (w/four Prongs).
| Device ID | K792100 |
| 510k Number | K792100 |
| Device Name: | GRASPING FORCEP (W/FOUR PRONGS) |
| Classification | Forceps, General & Plastic Surgery |
| Applicant | EDER INSTRUMENT CO, 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 | 1979-10-19 |
| Decision Date | 1979-11-13 |