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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 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 2022-07-12 under 510(k) 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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K220814.

When did NAEOTOM Alpha, Scan&GO Software receive FDA 510(k) clearance?

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

Who is the listed applicant for NAEOTOM Alpha, Scan&GO Software?

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 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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