The following data is part of a premarket notification filed by Dantec Medical, Inc. with the FDA for Dantec Electrodes Model Dne 116, 117 & 13p02/12.
| Device ID | K896874 |
| 510k Number | K896874 |
| Device Name: | DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 |
| Classification | Electrode, Needle, Diagnostic Electromyograph |
| Applicant | DANTEC MEDICAL, INC. 1575 EYE STREET, N.W. Washington, DC 20005 |
| Contact | Richard Manthei |
| Correspondent | Richard Manthei DANTEC MEDICAL, INC. 1575 EYE STREET, N.W. Washington, DC 20005 |
| Product Code | IKT |
| CFR Regulation Number | 890.1385 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-12-08 |
| Decision Date | 1990-06-18 |