Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BODY COMPOSITION ANALYZER

K-Number: K904970 · 1991-03-07

Decision Date1991-03-07
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BODY COMPOSITION ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Body Composition Analog, Inc.. It received FDA 510(k) clearance on 1991-03-07 under 510(k) number K904970. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODY COMPOSITION ANALYZER?

BODY COMPOSITION ANALYZER is a medical device that received FDA 510(k) clearance on 1991-03-07. The listed applicant is Body Composition Analog, Inc.. The 510(k) number is K904970.

When did BODY COMPOSITION ANALYZER receive FDA 510(k) clearance?

BODY COMPOSITION ANALYZER received FDA 510(k) clearance on 1991-03-07, under 510(k) number K904970.

Who is the listed applicant for BODY COMPOSITION ANALYZER?

The FDA 510(k) record lists Body Composition Analog, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BODY COMPOSITION ANALYZER?

The FDA product code for BODY COMPOSITION ANALYZER is DSB.

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 Body Composition Analog, Inc. 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.

Related Devices (Code: DSB)

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

View on FDA Database →

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

↑