CEDARA I-SOFTVIEW
K-Number: K022881 · 2002-10-22
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Device Summary
Frequently Asked Questions
What is the CEDARA I-SOFTVIEW?
CEDARA I-SOFTVIEW is a medical device that received FDA 510(k) clearance on 2002-10-22. The listed applicant is Cedara Software Corp.. The 510(k) number is K022881.
When did CEDARA I-SOFTVIEW receive FDA 510(k) clearance?
CEDARA I-SOFTVIEW received FDA 510(k) clearance on 2002-10-22, under 510(k) number K022881.
Who is the listed applicant for CEDARA I-SOFTVIEW?
The FDA 510(k) record lists Cedara Software Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CEDARA I-SOFTVIEW?
The FDA product code for CEDARA I-SOFTVIEW 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 Cedara Software 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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