The following data is part of a premarket notification filed by Medicotest, Inc. with the FDA for Cutaneous Electrode.
| Device ID | K931430 |
| 510k Number | K931430 |
| Device Name: | CUTANEOUS ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | MEDICOTEST, INC. ONE METROPOLITAN SQUARE 211 NORTH BROADWAY, SUITE 3600 St. Louis, MO 63102 |
| Contact | Randy Mariani |
| Correspondent | Randy Mariani MEDICOTEST, INC. ONE METROPOLITAN SQUARE 211 NORTH BROADWAY, SUITE 3600 St. Louis, MO 63102 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-03-22 |
| Decision Date | 1993-12-21 |