Class Class II

ARTIS icono (VE40A) (floor); ARTIS icono (VE40A) (biplane); ARTIS icono (VE40A) (ceiling); ARTIS pheno (VE40A) (K241572)

K241572 2024-10-22 Traditional
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Description

ARTIS icono (VE40A) (floor); ARTIS icono (VE40A) (biplane); ARTIS icono (VE40A) (ceiling); ARTIS pheno (VE40A) by Siemens Medical Solutions USA, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241572
Clearance Date2024-10-22
Clearance TypeTraditional
Product CodeOWB
Regulation Number892.1650

Categories

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Predicate lineage for K241572

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. ARTIS icono (VE40A) (floor); ARTIS icono (VE40A) (biplane); ARTIS icono (VE40A) (ceiling); ARTIS pheno (VE40A) (K241572) cites 3 predicate devices and is itself cited by 1 later device.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K230949ARTIS pheno (VE30A)Siemens Medical Solutions USA, Inc.2023
K230950ARTIS icono (VE30A)Siemens Medical Solutions USA, Inc.2023
K221516ARTIS icono (Ceiling Configuration)Siemens Medical Solutions USA, Inc.2022

Later devices that cite this one as their predicate

Devices that cite K241572
K numberDeviceApplicantYear
K254173ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling...Siemens Medical Solutions USA, Inc.2026

Trace the full predicate network for K241572

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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