The following data is part of a premarket notification filed by Conmed Corp. with the FDA for Conmed Electrosurgical Grounding Pads.
| Device ID | K942215 |
| 510k Number | K942215 |
| Device Name: | CONMED ELECTROSURGICAL GROUNDING PADS |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CONMED CORP. 310 BROAD ST. Utica, NY 13501 -1203 |
| Contact | Ira D Duesler Jr. |
| Correspondent | Ira D Duesler Jr. CONMED CORP. 310 BROAD ST. Utica, NY 13501 -1203 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-05-06 |
| Decision Date | 1994-05-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40653405033357 | K942215 | 000 |
| 40653405015971 | K942215 | 000 |
| 40653405015933 | K942215 | 000 |
| 40653405015919 | K942215 | 000 |
| 30653405015721 | K942215 | 000 |
| 30653405015691 | K942215 | 000 |
| 30653405030977 | K942215 | 000 |
| 20653405030970 | K942215 | 000 |
| 20653405031069 | K942215 | 000 |
| 40653405016022 | K942215 | 000 |
| 40653405016039 | K942215 | 000 |
| 40653405016060 | K942215 | 000 |
| 30653405031097 | K942215 | 000 |
| 30653405031080 | K942215 | 000 |
| 30653405031073 | K942215 | 000 |
| 30653405031066 | K942215 | 000 |
| 30653405031059 | K942215 | 000 |
| 30653405031035 | K942215 | 000 |
| 30653405030939 | K942215 | 000 |
| 40653405016077 | K942215 | 000 |
| 20653405031038 | K942215 | 000 |