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

AUTOTRANSFUSION APPARATUS

K Number: K873807 · Decision Mar 9, 1988
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
194
Applicant Total
21
Review Days
173

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Basic Information

Device Name
AUTOTRANSFUSION APPARATUS
K Number
K873807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5830
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Biodynamics Corp.
Date Received
September 18, 1987
Decision Date
March 9, 1988
Product Code
CAC
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAC Apparatus, Autotransfusion

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Other Clearances by Biodynamics Corp.

K Number Device Name
K051675 BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER
K884033 BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZER
K881631 BIODYNAMICS AUTOTRANSFUSION RESERVOIR
K881968 BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER
K874361 BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER
K874034 ADR-22 AUTOMATIC DIALYZER REPROCESSOR
K870052 INFUMIX MIXING CONTAINER
K822716 UNIVERSAL CENTRIFUGE
K822715 PLATELET CENTRIFUGE
K822422 BASIC CENTRIFUGE
Search all 21 clearances from Biodynamics Corp. →