ARTIS genio floor; ARTIS icono.explore floor
K-Number: K253752 · 2026-04-23
Device Summary
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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K253752.
When did ARTIS genio floor; ARTIS icono.explore floor receive FDA 510(k) clearance?
ARTIS genio floor; ARTIS icono.explore floor received FDA 510(k) clearance on 2026-04-23, under 510(k) number K253752.
Who is the listed applicant for ARTIS genio floor; ARTIS icono.explore floor?
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 genio floor; ARTIS icono.explore floor?
The FDA product code for ARTIS genio floor; ARTIS icono.explore floor 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.