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FDA 510(k)

INBODY, MODEL 3.0

K-Number: K042528 · 2005-01-11

ApplicantBiospace Corporation Limited
Decision Date2005-01-11
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INBODY, MODEL 3.0 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 2005-01-11 under 510(k) number K042528. 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, MODEL 3.0?

INBODY, MODEL 3.0 is a medical device that received FDA 510(k) clearance on 2005-01-11. The listed applicant is Biospace Corporation Limited. The 510(k) number is K042528.

When did INBODY, MODEL 3.0 receive FDA 510(k) clearance?

INBODY, MODEL 3.0 received FDA 510(k) clearance on 2005-01-11, under 510(k) number K042528.

Who is the listed applicant for INBODY, MODEL 3.0?

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, MODEL 3.0?

The FDA product code for INBODY, MODEL 3.0 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, R20BK062603BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230

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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 LimitedK130856BIA / VITALITY ANALYZERIpgdx, LLCK130952PRECISION 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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