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FDA 510(k)

BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER

K-Number: K051675 · 2006-03-16

ApplicantBiodynamics Corp.
Decision Date2006-03-16
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Biodynamics Corp.. It received FDA 510(k) clearance on 2006-03-16 under 510(k) number K051675. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER?

BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER is a medical device that received FDA 510(k) clearance on 2006-03-16. The listed applicant is Biodynamics Corp.. The 510(k) number is K051675.

When did BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER receive FDA 510(k) clearance?

BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER received FDA 510(k) clearance on 2006-03-16, under 510(k) number K051675.

Who is the listed applicant for BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER?

The FDA 510(k) record lists Biodynamics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER?

The FDA product code for BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER is MNW.

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Other records listing Biodynamics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K884033BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZERK881631BIODYNAMICS AUTOTRANSFUSION RESERVOIRK881968BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZERK874361BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZERK873807AUTOTRANSFUSION APPARATUSK874034ADR-22 AUTOMATIC DIALYZER REPROCESSOR

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Related Devices (Code: MNW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.K130856BIA / VITALITY ANALYZERIpgdx, LLCK130777INBODYBiospace Corporation LimitedK130952PRECISION ONE LIFECARE; DETECTO; DETECTOPrecision One Lifecare, Ltd.K131394TRANSTEK GLASS BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.K130311TRANSTEK BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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