TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418
K-Number: K033157 · 2004-04-08
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Device Summary
Frequently Asked Questions
What is the TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418?
TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418 is a medical device that received FDA 510(k) clearance on 2004-04-08. The listed applicant is Tanita Corp. of America. The 510(k) number is K033157.
When did TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418 receive FDA 510(k) clearance?
TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418 received FDA 510(k) clearance on 2004-04-08, under 510(k) number K033157.
Who is the listed applicant for TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418?
The FDA 510(k) record lists Tanita Corp. of America as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418?
The FDA product code for TANITA SEGMENTAL BODY COMPOSITION ANALYZER, MODEL BC-418 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.
Other records listing Tanita Corp. of America 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: 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
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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