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

BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER

K Number: K051675 · Decision Mar 16, 2006
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
78
Applicant Total
21
Review Days
266

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Basic Information

Device Name
BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER
K Number
K051675
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biodynamics Corp.
Date Received
June 23, 2005
Decision Date
March 16, 2006
Product Code
MNW
Advisory Committee
Cardiovascular
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
MNW Analyzer, Body Composition

Similar 510(k) Clearances

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Other Clearances by Biodynamics Corp.

K Number Device Name
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
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. →