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FDA 510(k)

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 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 2017-03-24 under 510(k) 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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K163297.

When did Scan&GO receive FDA 510(k) clearance?

Scan&GO received FDA 510(k) clearance on 2017-03-24, under 510(k) number K163297.

Who is the listed applicant for Scan&GO?

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 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.

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