STETHOFLUX— 510(k) K060064

Substantially Equivalent

Odvi

FDA 510(k) clearance K060064 for STETHOFLUX, Substantially Equivalent on 2006-04-10. Applicant: Odvi. Device class: 2.

Clearance details

Applicant: Odvi
Product code: Code JAF
Device class: Class 2
Regulation: 21 CFR 892.1540
Advisory panel: Radiology
Date received: 2006-01-09
Decision date: 2006-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orsay, FR

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.