FDA 510(k) Applications Submitted by MEDICOTEST, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970639 | 02/20/1997 | NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K | MEDICOTEST, INC. |
| K983597 | 10/13/1998 | NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES | MEDICOTEST, INC. |
| K961643 | 04/29/1996 | MEDICOTEST ECG ELECTRODES | MEDICOTEST, INC. |
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