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FDA 510(k)

ARTIS icono (VE21) System

K-Number: K220432 · 2022-06-29

Decision Date2022-06-29
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTIS icono (VE21) 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 2022-06-29 under 510(k) number K220432. 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 (VE21) System?

ARTIS icono (VE21) System is a medical device that received FDA 510(k) clearance on 2022-06-29. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K220432.

When did ARTIS icono (VE21) System receive FDA 510(k) clearance?

ARTIS icono (VE21) System received FDA 510(k) clearance on 2022-06-29, under 510(k) number K220432.

Who is the listed applicant for ARTIS icono (VE21) 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 ARTIS icono (VE21) System?

The FDA product code for ARTIS icono (VE21) System is OWB.

Other records listing Siemens Medical Solutions USA, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 252 devices →

Related Devices (Code: OWB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.