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FDA 510(k)

SOMATOM Perspective

K-Number: K151765 · 2016-03-25

Decision Date2016-03-25
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM Perspective is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-03-25 under approval number K151765. 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 Perspective?

SOMATOM Perspective is a medical device that received FDA 510(k) clearance on 2016-03-25. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K151765.

When was SOMATOM Perspective approved by the FDA?

SOMATOM Perspective received FDA 510(k) clearance on 2016-03-25, under approval number K151765.

What company makes SOMATOM Perspective?

SOMATOM Perspective is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for SOMATOM Perspective?

The FDA product code for SOMATOM Perspective is JAK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.