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Circadian, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K921878SCANMATE IIISeptember 11, 1992
K894956CIRCAMED HOLTER VERSION 4February 5, 1990
K874641CIRCADIAN STRESS TEST IIApril 1, 1988
K874155CIRCAMED MONITOR REMOTE START CONDUCTANCE METERNovember 23, 1987
K871251CIRCAMED FULL DISCLOSURE SYSTEMMay 22, 1987
K860973CIRCADIAN STRESS TEST SYSTEMAugust 25, 1986
K851517CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITOOctober 2, 1985
K851643REMOTE CONTROL MODULESeptember 9, 1985
K840741PULMONARY FUNCTION TESTING STSMarch 5, 1984
K833619CONDUCTANCE METERJanuary 27, 1984
K830830CIRCA MED TWO-CHANNELJune 18, 1983
K810698PHARMALOGApril 10, 1981
K800214CIRCAMED IFebruary 29, 1980