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FDA 510(k)

BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230

K-Number: K062603 · 2007-02-15

ApplicantBiospace Corporation Limited
Decision Date2007-02-15
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 is the device name listed in this FDA 510(k) record. The listed applicant is Biospace Corporation Limited. It received FDA 510(k) clearance on 2007-02-15 under 510(k) number K062603. 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 BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230?

BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 is a medical device that received FDA 510(k) clearance on 2007-02-15. The listed applicant is Biospace Corporation Limited. The 510(k) number is K062603.

When did BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 receive FDA 510(k) clearance?

BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 received FDA 510(k) clearance on 2007-02-15, under 510(k) number K062603.

Who is the listed applicant for BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230?

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

What is the FDA product code for BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230?

The FDA product code for BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 is MNW.

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Other records listing Biospace Corporation Limited 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.

K130777INBODYK131064BIOSPACEK123228INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B)K110689INBODYK092786INBODY, MODELS: 270, R20, R20BK052646BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20

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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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