NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER
K-Number: K061920 · 2006-08-21
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Device Summary
Frequently Asked Questions
What is the NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER?
NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER is a medical device that received FDA 510(k) clearance on 2006-08-21. The listed applicant is Novarad Corp.. The 510(k) number is K061920.
When did NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER receive FDA 510(k) clearance?
NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER received FDA 510(k) clearance on 2006-08-21, under 510(k) number K061920.
Who is the listed applicant for NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER?
The FDA 510(k) record lists Novarad Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER?
The FDA product code for NOVAPACS, NOVAVIEW, NOVACARDIO, NOVAQC AND NOVAER is LLZ.
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 Novarad Corp. 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: LLZ)
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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