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FDA 510(k)

BIA / VITALITY ANALYZER

K-Number: K130856 · 2013-11-25

ApplicantIpgdx, LLC
Decision Date2013-11-25
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIA / VITALITY ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Ipgdx, LLC. It received FDA 510(k) clearance on 2013-11-25 under 510(k) number K130856. 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 BIA / VITALITY ANALYZER?

BIA / VITALITY ANALYZER is a medical device that received FDA 510(k) clearance on 2013-11-25. The listed applicant is Ipgdx, LLC. The 510(k) number is K130856.

When did BIA / VITALITY ANALYZER receive FDA 510(k) clearance?

BIA / VITALITY ANALYZER received FDA 510(k) clearance on 2013-11-25, under 510(k) number K130856.

Who is the listed applicant for BIA / VITALITY ANALYZER?

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

What is the FDA product code for BIA / VITALITY ANALYZER?

The FDA product code for BIA / VITALITY ANALYZER is MNW.

Related Clinical Trials

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.

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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.K130777INBODYBiospace 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.K122388SECA MEDICAL BODY COMPOSTION ANALYZER 514, SECA MBCA 514, SECA MBCA, SECA 514Seca GmbH & Co. KG

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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