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FDA 510(k)

NAEOTOM Alpha, Scan&GO Software

K-Number: K220814 · 2022-07-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-07-12
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NAEOTOM Alpha, Scan&GO Software is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-07-12 under approval number K220814. 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 NAEOTOM Alpha, Scan&GO Software?

NAEOTOM Alpha, Scan&GO Software is a medical device that received FDA 510(k) clearance on 2022-07-12. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K220814.

When was NAEOTOM Alpha, Scan&GO Software approved by the FDA?

NAEOTOM Alpha, Scan&GO Software received FDA 510(k) clearance on 2022-07-12, under approval number K220814.

What company makes NAEOTOM Alpha, Scan&GO Software?

NAEOTOM Alpha, Scan&GO Software is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for NAEOTOM Alpha, Scan&GO Software?

The FDA product code for NAEOTOM Alpha, Scan&GO Software 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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