Cios Flow
K-Number: K203504 · 2020-12-22
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-12-22
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Cios Flow is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2020-12-22 under approval number K203504. 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 Flow?
Cios Flow is a medical device that received FDA 510(k) clearance on 2020-12-22. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K203504.
When was Cios Flow approved by the FDA?
Cios Flow received FDA 510(k) clearance on 2020-12-22, under approval number K203504.
What company makes Cios Flow?
Cios Flow is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Cios Flow?
The FDA product code for Cios Flow 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.