The following data is part of a premarket notification filed by Medtronic Andover Medical, Inc. with the FDA for Nortech Model 87202204 Electrode.
| Device ID | K903554 |
| 510k Number | K903554 |
| Device Name: | NORTECH MODEL 87202204 ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | MEDTRONIC ANDOVER MEDICAL, INC. 60 NEWARK ST. Haverhill, MA 01830 |
| Contact | Janice M Pevide |
| Correspondent | Janice M Pevide MEDTRONIC ANDOVER MEDICAL, INC. 60 NEWARK ST. Haverhill, MA 01830 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-08-07 |
| Decision Date | 1990-08-30 |