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FDA 510(k)

SOMATOM PROJECT 10-CT SCANNERS

K-Number: K991764 · 1999-08-17

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1999-08-17
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM PROJECT 10-CT SCANNERS 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 1999-08-17 under 510(k) number K991764. 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 SOMATOM PROJECT 10-CT SCANNERS?

SOMATOM PROJECT 10-CT SCANNERS is a medical device that received FDA 510(k) clearance on 1999-08-17. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K991764.

When did SOMATOM PROJECT 10-CT SCANNERS receive FDA 510(k) clearance?

SOMATOM PROJECT 10-CT SCANNERS received FDA 510(k) clearance on 1999-08-17, under 510(k) number K991764.

Who is the listed applicant for SOMATOM PROJECT 10-CT SCANNERS?

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 SOMATOM PROJECT 10-CT SCANNERS?

The FDA product code for SOMATOM PROJECT 10-CT SCANNERS 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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