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FDA 510(k)

BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT

K-Number: K994242 · 2000-03-15

ApplicantBodystat , Ltd.
Decision Date2000-03-15
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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 2000-03-15 under 510(k) number K994242. 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 BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT?

BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT is a medical device that received FDA 510(k) clearance on 2000-03-15. The listed applicant is Bodystat , Ltd.. The 510(k) number is K994242.

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

BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT received FDA 510(k) clearance on 2000-03-15, under 510(k) number K994242.

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

The FDA product code for BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT is MNW.

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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.

K082254MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNITK082255QUADSCAN 4000 BODY BODY COMPOSITION, FLUID & ILLNESS/SEGMENTAL MONITORING UNITK082253BODYSTAT 1500 BODY COMPOSITION MONITORING UNITK002835BODYSTATK980971BODYSTAT DUALSCAN 2005K971554BODYSTAT

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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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