The following data is part of a premarket notification filed by Kli with the FDA for Forceps, Electrosurgical.
| Device ID | K781109 |
| 510k Number | K781109 |
| Device Name: | FORCEPS, ELECTROSURGICAL |
| Classification | Coagulator-cutter, Endoscopic, Bipolar (and Accessories) |
| Applicant | KLI 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | HIN |
| CFR Regulation Number | 884.4150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-30 |
| Decision Date | 1978-09-14 |