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FDA 510(k)

TANITA BODY COMPOSITION ANALYZER, MODEL SC-331

K-Number: K090479 · 2009-07-07

ApplicantTanita Corporation of America
Decision Date2009-07-07
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TANITA BODY COMPOSITION ANALYZER, MODEL SC-331 is the device name listed in this FDA 510(k) record. The listed applicant is Tanita Corporation of America. It received FDA 510(k) clearance on 2009-07-07 under 510(k) number K090479. 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 TANITA BODY COMPOSITION ANALYZER, MODEL SC-331?

TANITA BODY COMPOSITION ANALYZER, MODEL SC-331 is a medical device that received FDA 510(k) clearance on 2009-07-07. The listed applicant is Tanita Corporation of America. The 510(k) number is K090479.

When did TANITA BODY COMPOSITION ANALYZER, MODEL SC-331 receive FDA 510(k) clearance?

TANITA BODY COMPOSITION ANALYZER, MODEL SC-331 received FDA 510(k) clearance on 2009-07-07, under 510(k) number K090479.

Who is the listed applicant for TANITA BODY COMPOSITION ANALYZER, MODEL SC-331?

The FDA 510(k) record lists Tanita Corporation of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TANITA BODY COMPOSITION ANALYZER, MODEL SC-331?

The FDA product code for TANITA BODY COMPOSITION ANALYZER, MODEL SC-331 is MNW.

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Other records listing Tanita Corporation of America 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.

K062652INNERSCAN BODY COMPOSITION MONITOR, INNERSCAN SEGMENTAL BODY COMPOSITION MONITOR

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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