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FDA 510(k)

MEDVIZER PACS, MODEL RELEASE 2000

K-Number: K000557 · 2000-04-24

ApplicantVitel Net
Decision Date2000-04-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDVIZER PACS, MODEL RELEASE 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Vitel Net. It received FDA 510(k) clearance on 2000-04-24 under 510(k) number K000557. 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 MEDVIZER PACS, MODEL RELEASE 2000?

MEDVIZER PACS, MODEL RELEASE 2000 is a medical device that received FDA 510(k) clearance on 2000-04-24. The listed applicant is Vitel Net. The 510(k) number is K000557.

When did MEDVIZER PACS, MODEL RELEASE 2000 receive FDA 510(k) clearance?

MEDVIZER PACS, MODEL RELEASE 2000 received FDA 510(k) clearance on 2000-04-24, under 510(k) number K000557.

Who is the listed applicant for MEDVIZER PACS, MODEL RELEASE 2000?

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

What is the FDA product code for MEDVIZER PACS, MODEL RELEASE 2000?

The FDA product code for MEDVIZER PACS, MODEL RELEASE 2000 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 Vitel Net 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.

K040581MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM

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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