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FDA 510(k)

INBODY, MODELS: 270, R20, R20B

K-Number: K092786 · 2010-03-10

ApplicantBiospace Corporation Limited
Decision Date2010-03-10
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INBODY, MODELS: 270, R20, R20B 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 2010-03-10 under 510(k) number K092786. 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 INBODY, MODELS: 270, R20, R20B?

INBODY, MODELS: 270, R20, R20B is a medical device that received FDA 510(k) clearance on 2010-03-10. The listed applicant is Biospace Corporation Limited. The 510(k) number is K092786.

When did INBODY, MODELS: 270, R20, R20B receive FDA 510(k) clearance?

INBODY, MODELS: 270, R20, R20B received FDA 510(k) clearance on 2010-03-10, under 510(k) number K092786.

Who is the listed applicant for INBODY, MODELS: 270, R20, R20B?

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 INBODY, MODELS: 270, R20, R20B?

The FDA product code for INBODY, MODELS: 270, R20, R20B 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)K110689INBODYK062603BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230K052646BIOSPACE 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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