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FDA 510(k)

COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM

K-Number: K940484 · 1994-04-19

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-04-19
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COROSKOP HI-P 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 1994-04-19 under 510(k) number K940484. 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 COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM?

COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K940484.

When did COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM receive FDA 510(k) clearance?

COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM received FDA 510(k) clearance on 1994-04-19, under 510(k) number K940484.

Who is the listed applicant for COROSKOP HI-P 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 COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM?

The FDA product code for COROSKOP HI-P 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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