Medicotest A/S

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020382BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIAJune 28, 2002
K020907NEUROLINE, SUBDERMAL NEEDLE ELECTRODESJune 14, 2002
K002079MULTI-FUNCTION DEFIBRILLATION ELECTRODEFebruary 22, 2001
K001869DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLESeptember 18, 2000
K983689BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODESJanuary 15, 1999
K983597NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODESJanuary 11, 1999
K973529NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODESNovember 20, 1997
K970639NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-KMay 15, 1997
K965194MEDICOM, TENS ELECTRODESMarch 6, 1997
K961643MEDICOTEST ECG ELECTRODESDecember 9, 1996
K952176DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-KSeptember 25, 1995
K941568K-10-VS, DA-05-VS, RECORDING ELECTRODESNovember 4, 1994
K931426NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODEDecember 21, 1993
K931430CUTANEOUS ELECTRODEDecember 21, 1993
K926264MEDICOTEST SKIN FIXApril 20, 1993
K921579BR-50-J DISPOSABLE ECG ELECTRODEMay 26, 1992
K914672QR-50-E DISPOSABLE RADIOTRANSLUCENT ECG ELECTRODEOctober 31, 1991
K902407NF-50-E DISPOSABLE ECG ELECTRODEJuly 31, 1990
K901280DISPOSIBLE EEG NEEDLE ELECTRODESMay 11, 1990
K821539MEDICOTEST ELECTRODE PASTEJuly 2, 1982