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FDA 510(k)

TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM

K-Number: K884788 · 1989-02-27

ApplicantToshiba Medical Systems
Decision Date1989-02-27
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM 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 1989-02-27 under 510(k) number K884788. 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-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM?

TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-02-27. The listed applicant is Toshiba Medical Systems. The 510(k) number is K884788.

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

TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM received FDA 510(k) clearance on 1989-02-27, under 510(k) number K884788.

Who is the listed applicant for TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM?

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-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM?

The FDA product code for TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM 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)

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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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