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FDA 510(k)

ARTIS genio floor; ARTIS icono.explore floor

K-Number: K253752 · 2026-04-23

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2026-04-23
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTIS genio floor; ARTIS icono.explore floor is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2026-04-23 under approval number K253752. 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 genio floor; ARTIS icono.explore floor?

ARTIS genio floor; ARTIS icono.explore floor is a medical device that received FDA 510(k) clearance on 2026-04-23. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K253752.

When was ARTIS genio floor; ARTIS icono.explore floor approved by the FDA?

ARTIS genio floor; ARTIS icono.explore floor received FDA 510(k) clearance on 2026-04-23, under approval number K253752.

What company makes ARTIS genio floor; ARTIS icono.explore floor?

ARTIS genio floor; ARTIS icono.explore floor is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for ARTIS genio floor; ARTIS icono.explore floor?

The FDA product code for ARTIS genio floor; ARTIS icono.explore floor 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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