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FDA 510(k)

COMMUNIFY PACS VIEWER

K-Number: K120851 · 2013-02-19

Decision Date2013-02-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMMUNIFY PACS VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Communify Health, LLC. It received FDA 510(k) clearance on 2013-02-19 under 510(k) number K120851. 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 COMMUNIFY PACS VIEWER?

COMMUNIFY PACS VIEWER is a medical device that received FDA 510(k) clearance on 2013-02-19. The listed applicant is Communify Health, LLC. The 510(k) number is K120851.

When did COMMUNIFY PACS VIEWER receive FDA 510(k) clearance?

COMMUNIFY PACS VIEWER received FDA 510(k) clearance on 2013-02-19, under 510(k) number K120851.

Who is the listed applicant for COMMUNIFY PACS VIEWER?

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

What is the FDA product code for COMMUNIFY PACS VIEWER?

The FDA product code for COMMUNIFY PACS VIEWER 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.

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

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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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