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Company · US

Medicotest A/S

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2002. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
IKT	Electrode, Needle, Diagnostic Electromyograph	3
DRX	Electrode, Electrocardiograph	2
GXY	Electrode, Cutaneous	1
MKJ	Automated External Defibrillators (Non-Wearable)	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jun 28, 2002	K020382	BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA Medicotest A/S	DRX
Jun 14, 2002	K020907	NEUROLINE, SUBDERMAL NEEDLE ELECTRODES Medicotest A/S	IKT
Feb 22, 2001	K002079	MULTI-FUNCTION DEFIBRILLATION ELECTRODE Medicotest A/S	MKJ
Sep 18, 2000	K001869	DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE Medicotest A/S	IKT
Jan 15, 1999	K983689	BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODES Medicotest A/S	DRX
Nov 20, 1997	K973529	NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODES Medicotest A/S	IKT
Mar 6, 1997	K965194	MEDICOM, TENS ELECTRODES Medicotest A/S	GXY

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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