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FDA 510(k)

TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY

K-Number: K863935 · 1986-12-02

ApplicantToshiba Medical Systems
Decision Date1986-12-02
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1986-12-02 under 510(k) number K863935. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY?

TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY is a medical device that received FDA 510(k) clearance on 1986-12-02. The listed applicant is Toshiba Medical Systems. The 510(k) number is K863935.

When did TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY receive FDA 510(k) clearance?

TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY received FDA 510(k) clearance on 1986-12-02, under 510(k) number K863935.

Who is the listed applicant for TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY?

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

What is the FDA product code for TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY?

The FDA product code for TOSHIBA TCT-600 COMPUTED TOMOGRAPHY (CT) X-RAY is JAK.

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Other records listing Toshiba Medical Systems as applicant

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K960948SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020AK954310BLA-800AK954309ANGIOREXK893750MRT-50A MOBILEK891453DIAGNOSTIC ULTRASOUND TRANSDUCER: PVE-582VK890969TRANSESOPHAGEAL TRANSDUCER PEF-511SA

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Related Devices (Code: JAK)

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.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, 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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