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FDA 510(k)

CLEARCANVAS RIS / PACS

K-Number: K110332 · 2011-03-24

ApplicantClearcanvas, Inc.
Decision Date2011-03-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLEARCANVAS RIS / PACS is the device name listed in this FDA 510(k) record. The listed applicant is Clearcanvas, Inc.. It received FDA 510(k) clearance on 2011-03-24 under 510(k) number K110332. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARCANVAS RIS / PACS?

CLEARCANVAS RIS / PACS is a medical device that received FDA 510(k) clearance on 2011-03-24. The listed applicant is Clearcanvas, Inc.. The 510(k) number is K110332.

When did CLEARCANVAS RIS / PACS receive FDA 510(k) clearance?

CLEARCANVAS RIS / PACS received FDA 510(k) clearance on 2011-03-24, under 510(k) number K110332.

Who is the listed applicant for CLEARCANVAS RIS / PACS?

The FDA 510(k) record lists Clearcanvas, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEARCANVAS RIS / PACS?

The FDA product code for CLEARCANVAS RIS / PACS is LLZ.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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