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FDA 510(k)

ARTIS icono (VE30A)

K-Number: K230950 · 2023-12-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2023-12-14
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTIS icono (VE30A) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2023-12-14 under approval number K230950. 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 (VE30A)?

ARTIS icono (VE30A) is a medical device that received FDA 510(k) clearance on 2023-12-14. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K230950.

When was ARTIS icono (VE30A) approved by the FDA?

ARTIS icono (VE30A) received FDA 510(k) clearance on 2023-12-14, under approval number K230950.

What company makes ARTIS icono (VE30A)?

ARTIS icono (VE30A) is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for ARTIS icono (VE30A)?

The FDA product code for ARTIS icono (VE30A) 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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