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FDA 510(k)

ARTIS ZEE AND ZEEGO

K-Number: K073290 · 2008-02-11

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2008-02-11
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTIS ZEE AND ZEEGO 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 2008-02-11 under 510(k) number K073290. 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 ARTIS ZEE AND ZEEGO?

ARTIS ZEE AND ZEEGO is a medical device that received FDA 510(k) clearance on 2008-02-11. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K073290.

When did ARTIS ZEE AND ZEEGO receive FDA 510(k) clearance?

ARTIS ZEE AND ZEEGO received FDA 510(k) clearance on 2008-02-11, under 510(k) number K073290.

Who is the listed applicant for ARTIS ZEE AND ZEEGO?

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 ARTIS ZEE AND ZEEGO?

The FDA product code for ARTIS ZEE AND ZEEGO 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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