Medicotest A/S is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medicotest A/S - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Medicotest A/S has 7 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 7 cleared submissions from 1997 to 2002. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medicotest A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicotest A/S
7 devices
Cleared
Jun 28, 2002
BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA
Cardiovascular
143d
Cleared
Jun 14, 2002
NEUROLINE, SUBDERMAL NEEDLE ELECTRODES
Neurology
86d
Cleared
Feb 22, 2001
MULTI-FUNCTION DEFIBRILLATION ELECTRODE
Cardiovascular
227d
Cleared
Sep 18, 2000
DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE
Neurology
90d
Cleared
Jan 15, 1999
BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODES
Cardiovascular
87d
Cleared
Nov 20, 1997
NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODES
Neurology
63d
Cleared
Mar 06, 1997
MEDICOM, TENS ELECTRODES
Neurology
72d