The following data is part of a premarket notification filed by Consolidated Medical Equipment, Inc. with the FDA for Conductive Adhesive Post-op Electrode-tens.
| Device ID | K850131 |
| 510k Number | K850131 |
| Device Name: | CONDUCTIVE ADHESIVE POST-OP ELECTRODE-TENS |
| Classification | Electrode, Cutaneous |
| Applicant | CONSOLIDATED MEDICAL EQUIPMENT, INC. 310 BROAD ST. Utica, NY 13501 |
| Contact | William W Abraham |
| Correspondent | William W Abraham CONSOLIDATED MEDICAL EQUIPMENT, INC. 310 BROAD ST. Utica, NY 13501 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-01-14 |
| Decision Date | 1985-03-05 |