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FDA 510(k)

MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM

K-Number: K930635 · 1993-09-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1993-09-07
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM 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 1993-09-07 under 510(k) number K930635. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM?

MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K930635.

When did MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM receive FDA 510(k) clearance?

MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM received FDA 510(k) clearance on 1993-09-07, under 510(k) number K930635.

Who is the listed applicant for MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM?

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 MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM?

The FDA product code for MULTISTAR D ANGIOGRAPHIC X-RAY SYSTEM is IZI.

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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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