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FDA 510(k)

VIEW(TM) IMAGE PROCESSING AND VIEWING STATION

K-Number: K864854 · 1987-02-26

ApplicantVirtual Imaging
Decision Date1987-02-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIEW(TM) IMAGE PROCESSING AND VIEWING STATION is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Imaging. It received FDA 510(k) clearance on 1987-02-26 under 510(k) number K864854. 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 VIEW(TM) IMAGE PROCESSING AND VIEWING STATION?

VIEW(TM) IMAGE PROCESSING AND VIEWING STATION is a medical device that received FDA 510(k) clearance on 1987-02-26. The listed applicant is Virtual Imaging. The 510(k) number is K864854.

When did VIEW(TM) IMAGE PROCESSING AND VIEWING STATION receive FDA 510(k) clearance?

VIEW(TM) IMAGE PROCESSING AND VIEWING STATION received FDA 510(k) clearance on 1987-02-26, under 510(k) number K864854.

Who is the listed applicant for VIEW(TM) IMAGE PROCESSING AND VIEWING STATION?

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

What is the FDA product code for VIEW(TM) IMAGE PROCESSING AND VIEWING STATION?

The FDA product code for VIEW(TM) IMAGE PROCESSING AND VIEWING STATION 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.

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Other records listing Virtual Imaging 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.

K063262AMX4-50 AND AMX4-31 MOBILE DIGITAL DIAGNOSTIC RADIOGRAPHIC SYSTEMSK922313P-LINKK891695VIEW 1000

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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