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FDA 510(k)

COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION

K-Number: K924985 · 1994-04-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-04-07
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1994-04-07 under 510(k) number K924985. 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 COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION?

COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION is a medical device that received FDA 510(k) clearance on 1994-04-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K924985.

When did COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION receive FDA 510(k) clearance?

COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION received FDA 510(k) clearance on 1994-04-07, under 510(k) number K924985.

Who is the listed applicant for COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION?

The FDA product code for COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION is 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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