Scan&GO
K-Number: K163297 · 2017-03-24
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2017-03-24
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Scan&GO is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2017-03-24 under approval number K163297. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Scan&GO?
Scan&GO is a medical device that received FDA 510(k) clearance on 2017-03-24. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K163297.
When was Scan&GO approved by the FDA?
Scan&GO received FDA 510(k) clearance on 2017-03-24, under approval number K163297.
What company makes Scan&GO?
Scan&GO is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Scan&GO?
The FDA product code for Scan&GO is JAK.
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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.