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FDA 510(k)

PROVIEW MEDICAL IMAGE DISPLAY MODULE

K-Number: K000770 · 2000-05-16

ApplicantCerner Corp.
Decision Date2000-05-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PROVIEW MEDICAL IMAGE DISPLAY MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Cerner Corp.. It received FDA 510(k) clearance on 2000-05-16 under 510(k) number K000770. 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 PROVIEW MEDICAL IMAGE DISPLAY MODULE?

PROVIEW MEDICAL IMAGE DISPLAY MODULE is a medical device that received FDA 510(k) clearance on 2000-05-16. The listed applicant is Cerner Corp.. The 510(k) number is K000770.

When did PROVIEW MEDICAL IMAGE DISPLAY MODULE receive FDA 510(k) clearance?

PROVIEW MEDICAL IMAGE DISPLAY MODULE received FDA 510(k) clearance on 2000-05-16, under 510(k) number K000770.

Who is the listed applicant for PROVIEW MEDICAL IMAGE DISPLAY MODULE?

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

What is the FDA product code for PROVIEW MEDICAL IMAGE DISPLAY MODULE?

The FDA product code for PROVIEW MEDICAL IMAGE DISPLAY MODULE is LLZ.

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Other records listing Cerner Corp. 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.

K121758CERNER FETALINK+(VERSION1.0)K093134CERNER CAREAWARE IBUSK091251CERNER FETALINK (VERSION 1.0)K091032CERNER PROVISION WORKSTATION (VERSION 2.5)K070394CERNER PROVISION WORKSTATIONK955000REMOTE VIEWING SYSTEM MEDICAL IMAGE DISPLAY MODULE

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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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