The following data is part of a premarket notification filed by Conmed Andover Medical, Inc. with the FDA for Cloth Tens/bnes Electrode.
| Device ID | K942718 |
| 510k Number | K942718 |
| Device Name: | CLOTH TENS/BNES ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | CONMED ANDOVER MEDICAL, INC. 60 NEWARK ST. Haverhill, MA 01832 -1398 |
| Contact | Brenda Cullinane |
| Correspondent | Brenda Cullinane CONMED ANDOVER MEDICAL, INC. 60 NEWARK ST. Haverhill, MA 01832 -1398 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-09 |
| Decision Date | 1994-09-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20653405016103 | K942718 | 000 |