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FDA 510(k)

SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX

K-Number: K875370 · 1988-05-18

ApplicantShimadzu Precision Instruments, Inc.
Decision Date1988-05-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Precision Instruments, Inc.. It received FDA 510(k) clearance on 1988-05-18 under 510(k) number K875370. 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 SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX?

SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX is a medical device that received FDA 510(k) clearance on 1988-05-18. The listed applicant is Shimadzu Precision Instruments, Inc.. The 510(k) number is K875370.

When did SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX receive FDA 510(k) clearance?

SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX received FDA 510(k) clearance on 1988-05-18, under 510(k) number K875370.

Who is the listed applicant for SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX?

The FDA 510(k) record lists Shimadzu Precision Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX?

The FDA product code for SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX is JAK.

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Other records listing Shimadzu Precision Instruments, Inc. as applicant

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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.

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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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