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FDA 510(k)

MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT

K-Number: K082254 · 2011-02-07

Decision Date2011-02-07
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Bodystat , Ltd.. It received FDA 510(k) clearance on 2011-02-07 under 510(k) number K082254. 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 MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT?

MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT is a medical device that received FDA 510(k) clearance on 2011-02-07. The listed applicant is Bodystat , Ltd.. The 510(k) number is K082254.

When did MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT receive FDA 510(k) clearance?

MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT received FDA 510(k) clearance on 2011-02-07, under 510(k) number K082254.

Who is the listed applicant for MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT?

The FDA 510(k) record lists Bodystat , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT?

The FDA product code for MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT 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 Bodystat , Ltd. 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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