AVITA BF1 (VITALIO) BODY FAT ANALYZER
K-Number: K020738 · 2003-05-22
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Device Summary
Frequently Asked Questions
What is the AVITA BF1 (VITALIO) BODY FAT ANALYZER?
AVITA BF1 (VITALIO) BODY FAT ANALYZER is a medical device that received FDA 510(k) clearance on 2003-05-22. The listed applicant is Avita Corporation. The 510(k) number is K020738.
When did AVITA BF1 (VITALIO) BODY FAT ANALYZER receive FDA 510(k) clearance?
AVITA BF1 (VITALIO) BODY FAT ANALYZER received FDA 510(k) clearance on 2003-05-22, under 510(k) number K020738.
Who is the listed applicant for AVITA BF1 (VITALIO) BODY FAT ANALYZER?
The FDA 510(k) record lists Avita Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVITA BF1 (VITALIO) BODY FAT ANALYZER?
The FDA product code for AVITA BF1 (VITALIO) BODY FAT ANALYZER 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 Avita Corporation 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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