Medicotest, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medicotest, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Medicotest, Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1982 to 1999. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medicotest, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicotest, Inc.
14 devices
Cleared
Jan 11, 1999
NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES
Neurology
90d
Cleared
May 15, 1997
NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S,...
Neurology
84d
Cleared
Dec 09, 1996
MEDICOTEST ECG ELECTRODES
Cardiovascular
224d
Cleared
Sep 25, 1995
DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K
Neurology
140d
Cleared
Nov 04, 1994
K-10-VS, DA-05-VS, RECORDING ELECTRODES
Neurology
218d
Cleared
Dec 21, 1993
NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE
Neurology
274d
Cleared
Dec 21, 1993
CUTANEOUS ELECTRODE
Neurology
274d
Cleared
Apr 20, 1993
MEDICOTEST SKIN FIX
General & Plastic Surgery
123d
Cleared
May 26, 1992
BR-50-J DISPOSABLE ECG ELECTRODE
Cardiovascular
54d
Cleared
Oct 31, 1991
QR-50-E DISPOSABLE RADIOTRANSLUCENT ECG ELECTRODE
Cardiovascular
13d
Cleared
Jul 31, 1990
NF-50-E DISPOSABLE ECG ELECTRODE
Cardiovascular
61d
Cleared
May 11, 1990
DISPOSIBLE EEG NEEDLE ELECTRODES
Neurology
53d