BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010
K-Number: K863833 · 1987-03-17
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Device Summary
Frequently Asked Questions
What is the BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010?
BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010 is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is Body Watch, Inc.. The 510(k) number is K863833.
When did BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010 receive FDA 510(k) clearance?
BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010 received FDA 510(k) clearance on 1987-03-17, under 510(k) number K863833.
Who is the listed applicant for BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010?
The FDA 510(k) record lists Body Watch, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010?
The FDA product code for BODY WATCH BODY COMPOSITION ANALYZER MODEL 2010 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.
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.
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