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FDA 510(k)

MIP/CT IMAGE PROCESSING WORKSTATION

K-Number: K892712 · 1989-10-19

ApplicantKontron Electronics
Decision Date1989-10-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIP/CT IMAGE PROCESSING WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Electronics. It received FDA 510(k) clearance on 1989-10-19 under 510(k) number K892712. 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 MIP/CT IMAGE PROCESSING WORKSTATION?

MIP/CT IMAGE PROCESSING WORKSTATION is a medical device that received FDA 510(k) clearance on 1989-10-19. The listed applicant is Kontron Electronics. The 510(k) number is K892712.

When did MIP/CT IMAGE PROCESSING WORKSTATION receive FDA 510(k) clearance?

MIP/CT IMAGE PROCESSING WORKSTATION received FDA 510(k) clearance on 1989-10-19, under 510(k) number K892712.

Who is the listed applicant for MIP/CT IMAGE PROCESSING WORKSTATION?

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

What is the FDA product code for MIP/CT IMAGE PROCESSING WORKSTATION?

The FDA product code for MIP/CT IMAGE PROCESSING WORKSTATION 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 Kontron Electronics 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.

K891689MIPRON/UMIPRONK891692MIP MR

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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