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FDA 510(k)

Cios Spin

K-Number: K181550 · 2018-10-30

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2018-10-30
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Cios Spin is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2018-10-30 under approval number K181550. 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 2018-10-30. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K181550.

When was Cios Spin approved by the FDA?

Cios Spin received FDA 510(k) clearance on 2018-10-30, under approval number K181550.

What company makes Cios Spin?

Cios Spin is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for Cios Spin?

The FDA product code for Cios Spin 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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