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FDA 510(k)

ARTIS icono (Ceiling Configuration)

K-Number: K221516 · 2022-07-19

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-07-19
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTIS icono (Ceiling Configuration) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-07-19 under approval number K221516. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTIS icono (Ceiling Configuration)?

ARTIS icono (Ceiling Configuration) is a medical device that received FDA 510(k) clearance on 2022-07-19. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K221516.

When was ARTIS icono (Ceiling Configuration) approved by the FDA?

ARTIS icono (Ceiling Configuration) received FDA 510(k) clearance on 2022-07-19, under approval number K221516.

What company makes ARTIS icono (Ceiling Configuration)?

ARTIS icono (Ceiling Configuration) is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for ARTIS icono (Ceiling Configuration)?

The FDA product code for ARTIS icono (Ceiling Configuration) is OWB.

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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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