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FDA 510(k)

Cios Select

K-Number: K250241 · 2025-11-04

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2025-11-04
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Cios Select 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 2025-11-04 under 510(k) number K250241. 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 Cios Select?

Cios Select is a medical device that received FDA 510(k) clearance on 2025-11-04. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K250241.

When did Cios Select receive FDA 510(k) clearance?

Cios Select received FDA 510(k) clearance on 2025-11-04, under 510(k) number K250241.

Who is the listed applicant for Cios Select?

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 Cios Select?

The FDA product code for Cios Select is OWB.

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Related Devices (Code: 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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