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FDA 510(k)

MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR

K-Number: K873580 · 1987-11-02

ApplicantMedical High Technology International, Inc.
Decision Date1987-11-02
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical High Technology International, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873580. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR?

MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Medical High Technology International, Inc.. The 510(k) number is K873580.

When did MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR receive FDA 510(k) clearance?

MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873580.

Who is the listed applicant for MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR?

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

What is the FDA product code for MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR?

The FDA product code for MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR is KPQ.

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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Related Devices (Code: KPQ)

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.

K132045ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONSGe Hungary KftK101038RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGERAcceletronics Digital Imaging, LLCK090706ONCENTRA SIMULATION 2.3Nucletron CorporationK083591IKOENGELO, VERSION 2Ikoetech, LLCK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALNucletron Corp.K061006IKOENGELOIkoetech, 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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