The following data is part of a premarket notification filed by Concept, Inc. with the FDA for Bipolar Forceps.
| Device ID | K792365 |
| 510k Number | K792365 |
| Device Name: | BIPOLAR FORCEPS |
| Classification | Electrode, Electrosurgical |
| Applicant | CONCEPT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JOS |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-23 |
| Decision Date | 1979-12-10 |