The following data is part of a premarket notification filed by Premier Dental Products Co. with the FDA for Electrosurgical Electrodes.
| Device ID | K923332 |
| 510k Number | K923332 |
| Device Name: | ELECTROSURGICAL ELECTRODES |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | PREMIER DENTAL PRODUCTS CO. 1710 ROMANO DR. P.O. BOX 111 Norristown, PA 19401 |
| Contact | William J Frezel |
| Correspondent | William J Frezel PREMIER DENTAL PRODUCTS CO. 1710 ROMANO DR. P.O. BOX 111 Norristown, PA 19401 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-07-07 |
| Decision Date | 1992-10-13 |