Medical Device Manufacturer · US , Washington , DC

Medicotest A/S - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1997

Recent clearances: BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODES, NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODES, MEDICOM, TENS ELECTRODES

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.

Medicotest A/S is one of 7689 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medicotest A/S

7 devices

1-7 of 7

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