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FDA 510(k)

SOMATOM DRI X-RAY CT SCANNER

K-Number: K837107 · 1983-03-09

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1983-03-09
Product Code
DecisionSubstantially Equivalent

Device Summary

SOMATOM DRI X-RAY CT SCANNER 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 1983-03-09 under 510(k) number K837107. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOMATOM DRI X-RAY CT SCANNER?

SOMATOM DRI X-RAY CT SCANNER is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K837107.

When did SOMATOM DRI X-RAY CT SCANNER receive FDA 510(k) clearance?

SOMATOM DRI X-RAY CT SCANNER received FDA 510(k) clearance on 1983-03-09, under 510(k) number K837107.

Who is the listed applicant for SOMATOM DRI X-RAY CT SCANNER?

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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