FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SCANMATE III

K Number: K921878 · Decision Sep 11, 1992
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
2
Applicant Total
13
Review Days
144

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Basic Information

Device Name
SCANMATE III
K Number
K921878
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1370
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Circadian, Inc.
Date Received
April 20, 1992
Decision Date
September 11, 1992
Product Code
IYP
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IYP Phantom, Anthropomorphic, Nuclear

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Other Clearances by Circadian, Inc.

K Number Device Name
K894956 CIRCAMED HOLTER VERSION 4
K874641 CIRCADIAN STRESS TEST II
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. →