The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Scotchplate Ii Dispersive Electrode.
| Device ID | K833364 |
| 510k Number | K833364 |
| Device Name: | 3M SCOTCHPLATE II DISPERSIVE ELECTRODE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | 3M COMPANY 2724 SOUTH PECK RD. Monrovia, CA 91016 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-28 |
| Decision Date | 1983-11-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50707387563504 | K833364 | 000 |
| 50707387454628 | K833364 | 000 |
| 50707387092707 | K833364 | 000 |
| 50707387092691 | K833364 | 000 |
| 50707387079906 | K833364 | 000 |
| 50707387033328 | K833364 | 000 |
| 04064035032814 | K833364 | 000 |