AVANZA
K-Number: K060870 · 2006-05-15
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Device Summary
Frequently Asked Questions
What is the AVANZA?
AVANZA is a medical device that received FDA 510(k) clearance on 2006-05-15. The listed applicant is Mds Nordion. The 510(k) number is K060870.
When did AVANZA receive FDA 510(k) clearance?
AVANZA received FDA 510(k) clearance on 2006-05-15, under 510(k) number K060870.
Who is the listed applicant for AVANZA?
The FDA 510(k) record lists Mds Nordion as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVANZA?
The FDA product code for AVANZA is JAI.
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 Mds Nordion 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: JAI)
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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