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FDA 510(k)

SOMATOM go.Up, SOMATOM go.Now

K-Number: K163296 · 2017-03-21

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2017-03-21
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM go.Up, SOMATOM go.Now is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2017-03-21 under approval number K163296. 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 SOMATOM go.Up, SOMATOM go.Now?

SOMATOM go.Up, SOMATOM go.Now is a medical device that received FDA 510(k) clearance on 2017-03-21. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K163296.

When was SOMATOM go.Up, SOMATOM go.Now approved by the FDA?

SOMATOM go.Up, SOMATOM go.Now received FDA 510(k) clearance on 2017-03-21, under approval number K163296.

What company makes SOMATOM go.Up, SOMATOM go.Now?

SOMATOM go.Up, SOMATOM go.Now is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for SOMATOM go.Up, SOMATOM go.Now?

The FDA product code for SOMATOM go.Up, SOMATOM go.Now 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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