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FDA 510(k)

CEMAX VIPSTATION AND/OR SOFTWARE

K-Number: K945188 · 1995-08-02

ApplicantCemax, Inc.
Decision Date1995-08-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEMAX VIPSTATION AND/OR SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Cemax, Inc.. It received FDA 510(k) clearance on 1995-08-02 under 510(k) number K945188. 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 CEMAX VIPSTATION AND/OR SOFTWARE?

CEMAX VIPSTATION AND/OR SOFTWARE is a medical device that received FDA 510(k) clearance on 1995-08-02. The listed applicant is Cemax, Inc.. The 510(k) number is K945188.

When did CEMAX VIPSTATION AND/OR SOFTWARE receive FDA 510(k) clearance?

CEMAX VIPSTATION AND/OR SOFTWARE received FDA 510(k) clearance on 1995-08-02, under 510(k) number K945188.

Who is the listed applicant for CEMAX VIPSTATION AND/OR SOFTWARE?

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

What is the FDA product code for CEMAX VIPSTATION AND/OR SOFTWARE?

The FDA product code for CEMAX VIPSTATION AND/OR SOFTWARE is LLZ.

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Other records listing Cemax, Inc. 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.

K950513ARCHIVEMANAGERK943357CEMAX SCANLINK VK932371CEMAX CLINICALVIEW(TM) STATION AND/OR SOFTWAREK932372CEMAX VIPSTATION(TM) AND/OR SOFTWAREK905801CEMAX SPARCSTATION IMAGING SOFTWARE AND WORKSTATIOK880169CEMAX 5000 MULTIDIMENSIONAL IMAGING WORKSTATION

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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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