Class Class II

NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime (K243523)

K243523 2025-02-12 Traditional
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Description

NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime by Siemens Medical Solutions USA, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243523
Clearance Date2025-02-12
Clearance TypeTraditional
Product CodeJAK
Regulation Number892.1750

Categories

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Predicate lineage for K243523

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime (K243523) cites 2 predicate devices and is itself cited by 1 later device.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K233657NAEOTOM AlphaSiemens Medical Solutions USA, Inc.2024
K233650SOMATOM go.Up; SOMATOM go.Now; SOMATOM go.All; SOMATOM go.T...Siemens Medical Solutions USA, Inc.2024

Later devices that cite this one as their predicate

Devices that cite K243523
K numberDeviceApplicantYear
K251061NAEOTOM Alpha.Peak/NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTO...Siemens Medical Solutions USA, Inc.2025

Trace the full predicate network for K243523

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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