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FDA 510(k)

ARTISTE MV SA

K-Number: K072485 · 2007-12-27

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2007-12-27
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTISTE MV SA 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 2007-12-27 under 510(k) number K072485. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTISTE MV SA?

ARTISTE MV SA is a medical device that received FDA 510(k) clearance on 2007-12-27. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K072485.

When did ARTISTE MV SA receive FDA 510(k) clearance?

ARTISTE MV SA received FDA 510(k) clearance on 2007-12-27, under 510(k) number K072485.

Who is the listed applicant for ARTISTE MV SA?

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 ARTISTE MV SA?

The FDA product code for ARTISTE MV SA is IYE.

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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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