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FDA 510(k)

ANGIO-CT MIYABI

K-Number: K990491 · 1999-04-05

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1999-04-05
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIO-CT MIYABI 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 1999-04-05 under 510(k) number K990491. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIO-CT MIYABI?

ANGIO-CT MIYABI is a medical device that received FDA 510(k) clearance on 1999-04-05. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K990491.

When did ANGIO-CT MIYABI receive FDA 510(k) clearance?

ANGIO-CT MIYABI received FDA 510(k) clearance on 1999-04-05, under 510(k) number K990491.

Who is the listed applicant for ANGIO-CT MIYABI?

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 ANGIO-CT MIYABI?

The FDA product code for ANGIO-CT MIYABI is IXI.

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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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