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FDA 510(k)

Cios Connect

K-Number: K153147 · 2016-01-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2016-01-12
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Cios Connect 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 2016-01-12 under 510(k) number K153147. 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 Connect?

Cios Connect is a medical device that received FDA 510(k) clearance on 2016-01-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K153147.

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

Cios Connect received FDA 510(k) clearance on 2016-01-12, under 510(k) number K153147.

Who is the listed applicant for Cios Connect?

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 Connect?

The FDA product code for Cios Connect 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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