Medicotest, Inc.
Medicotest, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1999.
Top product codes for Medicotest, Inc.
Recent clearances by Medicotest, Inc.
- K983597 — NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES
- K970639 — NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K
- K961643 — MEDICOTEST ECG ELECTRODES
- K952176 — DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K
- K941568 — K-10-VS, DA-05-VS, RECORDING ELECTRODES
- K931426 — NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE
- K931430 — CUTANEOUS ELECTRODE
- K926264 — MEDICOTEST SKIN FIX
- K921579 — BR-50-J DISPOSABLE ECG ELECTRODE
- K914672 — QR-50-E DISPOSABLE RADIOTRANSLUCENT ECG ELECTRODE
- K902407 — NF-50-E DISPOSABLE ECG ELECTRODE
- K901280 — DISPOSIBLE EEG NEEDLE ELECTRODES
- K821539 — MEDICOTEST ELECTRODE PASTE
- K821506 — MEDICOTEST ECG ELECTRODES
Data sourced from openFDA. This site is unofficial and independent of the FDA.