Sentry Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K962122SENTRY RADIOTRANSLUCENT ECG ELECTRODESJuly 24, 1996
K955636SENTRY DISPOSABLE DISPERSIVE ELECTRODEMarch 27, 1996
K942827SENTRY INSERTION TRAYNovember 2, 1994
K934000SENTRY AQUEOUS GEL ECG ELECTRODESAugust 30, 1994
K935098BABY BOARDFebruary 15, 1994
K933603LEADWIREJanuary 18, 1994
K932704PATIENT CABLEDecember 27, 1993
K881670ACCUTEMP PLUSNovember 22, 1988
K881343DURADERM BUTTERFLYMay 4, 1988
K851522DIAGNOSTIC ECG DISPOSABLE ELECTRODEOctober 24, 1985
K853552SENTRY FLEXIBLE TENSSeptember 26, 1985
K844632INFANT LIMB ELECTRODEJanuary 14, 1985
K830362INFANT ELECTRODE BELTJune 3, 1983