AVANZA— 510(k) K060870

Substantially Equivalent

Mds Nordion

FDA 510(k) clearance K060870 for AVANZA, Substantially Equivalent on 2006-05-15. Applicant: Mds Nordion. Device class: 2.

Clearance details

Applicant: Mds Nordion
Product code: Code JAI
Device class: Class 2
Regulation: 21 CFR 892.5770
Advisory panel: Radiology
Date received: 2006-03-30
Decision date: 2006-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ottawa, CA

Download summary PDF View on FDA.gov ↗

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