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FDA 510(k)

IMAGESVR PACS

K-Number: K082808 · 2009-01-09

ApplicantJaguar Technology Limited
Decision Date2009-01-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGESVR PACS is the device name listed in this FDA 510(k) record. The listed applicant is Jaguar Technology Limited. It received FDA 510(k) clearance on 2009-01-09 under 510(k) number K082808. 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 IMAGESVR PACS?

IMAGESVR PACS is a medical device that received FDA 510(k) clearance on 2009-01-09. The listed applicant is Jaguar Technology Limited. The 510(k) number is K082808.

When did IMAGESVR PACS receive FDA 510(k) clearance?

IMAGESVR PACS received FDA 510(k) clearance on 2009-01-09, under 510(k) number K082808.

Who is the listed applicant for IMAGESVR PACS?

The FDA 510(k) record lists Jaguar Technology Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMAGESVR PACS?

The FDA product code for IMAGESVR 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.

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

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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