ClearanceBrief
Company ยท US

Circadian, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1992. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DPSElectrocardiograph4
DSIDetector And Alarm, Arrhythmia3
DSHRecorder, Magnetic Tape, Medical2
KRCTester, Electrode, Surface, Electrocardiographic2
BZGSpirometer, Diagnostic1
IYPPhantom, Anthropomorphic, Nuclear1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 11, 1992K921878SCANMATE III
Circadian, Inc.
IYP
Feb 5, 1990K894956CIRCAMED HOLTER VERSION 4
Circadian, Inc.
DPS
Apr 1, 1988K874641CIRCADIAN STRESS TEST II
Circadian, Inc.
DPS
Nov 23, 1987K874155CIRCAMED MONITOR REMOTE START CONDUCTANCE METER
Circadian, Inc.
KRC
May 22, 1987K871251CIRCAMED FULL DISCLOSURE SYSTEM
Circadian, Inc.
DSI
Aug 25, 1986K860973CIRCADIAN STRESS TEST SYSTEM
Circadian, Inc.
DPS
Oct 2, 1985K851517CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO
Circadian, Inc.
DSI
Sep 9, 1985K851643REMOTE CONTROL MODULE
Circadian, Inc.
DPS
Mar 5, 1984K840741PULMONARY FUNCTION TESTING STS
Circadian, Inc.
BZG
Jan 27, 1984K833619CONDUCTANCE METER
Circadian, Inc.
KRC
Jun 18, 1983K830830CIRCA MED TWO-CHANNEL
Circadian, Inc.
DSI
Apr 10, 1981K810698PHARMALOG
Circadian, Inc.
DSH
Feb 29, 1980K800214CIRCAMED I
Circadian, Inc.
DSH

Latest recalls

DateFirm and productCodeLinked 510(k)
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