The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Scotchplate 51148 Small Conductive.
| Device ID | K823689 |
| 510k Number | K823689 |
| Device Name: | 3M SCOTCHPLATE 51148 SMALL CONDUCTIVE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | 3M COMPANY 8124 PACIFIC AVE. White City, OR 97503 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-07 |
| Decision Date | 1983-01-12 |