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 |