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FDA 510(k)

Cios Spin

K-Number: K251523 · 2025-07-29

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2025-07-29
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Cios Spin 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 2025-07-29 under 510(k) number K251523. 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 Spin?

Cios Spin is a medical device that received FDA 510(k) clearance on 2025-07-29. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K251523.

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

Cios Spin received FDA 510(k) clearance on 2025-07-29, under 510(k) number K251523.

Who is the listed applicant for Cios Spin?

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 Spin?

The FDA product code for Cios Spin is OWB.

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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.

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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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