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Cambridge Medical Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K896771EKG, ECG KENZ, ECG 302February 26, 1990
K896772EKG, ECG KENZ, ECG 303February 26, 1990
K895961MODEL MC6500 ELECTROCARDIOGRAPHJanuary 4, 1990
K883454MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPHJanuary 25, 1989
K871993MC 6000 MULTI-CHANNEL ELECTROCARDIOGRAPHNovember 23, 1987
K862748MODEL SC-1000 ELECTROCARDIOGRAPH SPECIFICATIONAugust 25, 1986
K854282PREVIEW XTJanuary 8, 1986
K854283CAMBRIDGE MODEL XT1000November 13, 1985