Cios Select
K-Number: K153232 · 2016-02-10
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2016-02-10
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Cios Select is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-02-10 under approval number K153232. 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 2016-02-10. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K153232.
When was Cios Select approved by the FDA?
Cios Select received FDA 510(k) clearance on 2016-02-10, under approval number K153232.
What company makes Cios Select?
Cios Select is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Cios Select?
The FDA product code for Cios Select is OWB.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: OWB)
K162859Allura Xper FD series and Allura Xper OR Table seriesPhilips Medical Systems Nederland B.V.
K162148Allura Xper R9Philips Medical Systems Nethrlands BV
K162614Infinix, INFX-8000V, V6.35Toshibamedical Systems Corporation
K160279ANYVIEW-500R Fluoroscopic Mobile X-Ray SystemEcotron Co., Ltd.
K161976Ziehm Solo FDZiehm Imaging GmbH
K161756SyncVision SystemVolcano Corporation
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.