The following data is part of a premarket notification filed by Delta Medical Electronics, Inc. with the FDA for Delta Conductive Adhesive Electrosurg-.
| Device ID | K832157 |
| 510k Number | K832157 |
| Device Name: | DELTA CONDUCTIVE ADHESIVE ELECTROSURG- |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | DELTA MEDICAL ELECTRONICS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-07-05 |
| Decision Date | 1983-07-26 |