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FDA 510(k)

HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960

K-Number: K030349 · 2003-05-02

Decision Date2003-05-02
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960 is the device name listed in this FDA 510(k) record. The listed applicant is Bonso Electronics International, Inc.. It received FDA 510(k) clearance on 2003-05-02 under 510(k) number K030349. 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 HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960?

HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960 is a medical device that received FDA 510(k) clearance on 2003-05-02. The listed applicant is Bonso Electronics International, Inc.. The 510(k) number is K030349.

When did HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960 receive FDA 510(k) clearance?

HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960 received FDA 510(k) clearance on 2003-05-02, under 510(k) number K030349.

Who is the listed applicant for HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960?

The FDA 510(k) record lists Bonso Electronics International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960?

The FDA product code for HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960 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.

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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