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 |