FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CIRCADIAN STRESS TEST II

K Number: K874641 · Decision Apr 1, 1988
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
13
Review Days
140

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Basic Information

Device Name
CIRCADIAN STRESS TEST II
K Number
K874641
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Circadian, Inc.
Date Received
November 13, 1987
Decision Date
April 1, 1988
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPS Electrocardiograph

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Other Clearances by Circadian, Inc.

K Number Device Name
K921878 SCANMATE III
K894956 CIRCAMED HOLTER VERSION 4
K874155 CIRCAMED MONITOR REMOTE START CONDUCTANCE METER
K871251 CIRCAMED FULL DISCLOSURE SYSTEM
K860973 CIRCADIAN STRESS TEST SYSTEM
K851517 CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO
K851643 REMOTE CONTROL MODULE
K840741 PULMONARY FUNCTION TESTING STS
K833619 CONDUCTANCE METER
K830830 CIRCA MED TWO-CHANNEL
Search all 13 clearances from Circadian, Inc. →