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FDA 510(k)

TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS

K-Number: K853444 · 1985-11-08

ApplicantToshiba Medical Systems
Decision Date1985-11-08
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS 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 1985-11-08 under 510(k) number K853444. 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-900S COMPUTED TOMOGRAPHY CT X-RAY SYS?

TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Toshiba Medical Systems. The 510(k) number is K853444.

When did TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS receive FDA 510(k) clearance?

TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS received FDA 510(k) clearance on 1985-11-08, under 510(k) number K853444.

Who is the listed applicant for TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS?

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-900S COMPUTED TOMOGRAPHY CT X-RAY SYS?

The FDA product code for TOSHIBA TCT-900S COMPUTED TOMOGRAPHY CT X-RAY SYS is JAK.

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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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