MODIFIED SONAMET BODY COMPOSITION ANALYZER
K-Number: K032610 · 2004-03-01
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Device Summary
Frequently Asked Questions
What is the MODIFIED SONAMET BODY COMPOSITION ANALYZER?
MODIFIED SONAMET BODY COMPOSITION ANALYZER is a medical device that received FDA 510(k) clearance on 2004-03-01. The listed applicant is Life Measurement, Inc.. The 510(k) number is K032610.
When did MODIFIED SONAMET BODY COMPOSITION ANALYZER receive FDA 510(k) clearance?
MODIFIED SONAMET BODY COMPOSITION ANALYZER received FDA 510(k) clearance on 2004-03-01, under 510(k) number K032610.
Who is the listed applicant for MODIFIED SONAMET BODY COMPOSITION ANALYZER?
The FDA 510(k) record lists Life Measurement, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED SONAMET BODY COMPOSITION ANALYZER?
The FDA product code for MODIFIED SONAMET BODY COMPOSITION ANALYZER is OAC.
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 Life Measurement, 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: OAC)
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.
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