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

BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER

K Number: K881968 · Decision Jul 28, 1988
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
113
Applicant Total
21
Review Days
78

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Basic Information

Device Name
BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER
K Number
K881968
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Biodynamics Corp.
Date Received
May 11, 1988
Decision Date
July 28, 1988
Product Code
DSB
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
DSB Plethysmograph, Impedance

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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
K874361 BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER
K873807 AUTOTRANSFUSION APPARATUS
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. →