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FDA 510(k)

CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY

K-Number: K945838 · 1995-10-25

ApplicantToshiba America Medical Systems, In.C
Decision Date1995-10-25
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1995-10-25 under 510(k) number K945838. 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 CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY?

CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY is a medical device that received FDA 510(k) clearance on 1995-10-25. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K945838.

When did CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY receive FDA 510(k) clearance?

CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY received FDA 510(k) clearance on 1995-10-25, under 510(k) number K945838.

Who is the listed applicant for CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY?

The FDA product code for CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY is KPQ.

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Other records listing Toshiba America Medical Systems, In.C 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.

K132106INFINIX ANGIO WORKSTATION W/DTS SOFTWAREK131822ULTRAEXTEND USWS-900A V2.1 AND V3.1K123097DOSE TRACKING SYSTEM MODEL XIDF-DTS801K122613VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/USK121076ULTRAEXTEND FX, ULTRASOUND WORKSTATION PACKAGEK122842RADREX-I, SW V4.00 MODEL DRAD-3000E

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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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