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FDA 510(k)

BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20

K-Number: K052646 · 2005-12-16

Decision Date2005-12-16
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 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 2005-12-16 under 510(k) number K052646. 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, MODELS INBODY 520, 720 AND S20?

BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Biospace Corporation Limited. The 510(k) number is K052646.

When did BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 receive FDA 510(k) clearance?

BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 received FDA 510(k) clearance on 2005-12-16, under 510(k) number K052646.

Who is the listed applicant for BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20?

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, MODELS INBODY 520, 720 AND S20?

The FDA product code for BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 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.

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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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