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FDA 510(k)

CENTRICITY PACS WEB DIAGNOSTIC

K-Number: K083018 · 2008-11-14

ApplicantGe Healthcare Dynamic Imaging Solutions
Decision Date2008-11-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CENTRICITY PACS WEB DIAGNOSTIC is the device name listed in this FDA 510(k) record. The listed applicant is Ge Healthcare Dynamic Imaging Solutions. It received FDA 510(k) clearance on 2008-11-14 under 510(k) number K083018. 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 CENTRICITY PACS WEB DIAGNOSTIC?

CENTRICITY PACS WEB DIAGNOSTIC is a medical device that received FDA 510(k) clearance on 2008-11-14. The listed applicant is Ge Healthcare Dynamic Imaging Solutions. The 510(k) number is K083018.

When did CENTRICITY PACS WEB DIAGNOSTIC receive FDA 510(k) clearance?

CENTRICITY PACS WEB DIAGNOSTIC received FDA 510(k) clearance on 2008-11-14, under 510(k) number K083018.

Who is the listed applicant for CENTRICITY PACS WEB DIAGNOSTIC?

The FDA 510(k) record lists Ge Healthcare Dynamic Imaging Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRICITY PACS WEB DIAGNOSTIC?

The FDA product code for CENTRICITY PACS WEB DIAGNOSTIC is LLZ.

Related Clinical Trials

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Other records listing Ge Healthcare Dynamic Imaging Solutions 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.

K082318CENTRICITY PACS IW

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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