Class Class II

V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System (K223387)

K223387 2023-02-13 Traditional
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Description

V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System by Samsung Medison Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223387
Clearance Date2023-02-13
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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Predicate lineage for K223387

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. V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System (K223387) cites 4 predicate devices and is itself cited by 4 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K220975V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound S...Samsung Medison Co., Ltd.2022
K221117RS85 Diagnostic Ultrasound System, RS80 EVO Diagnostic Ultr...Samsung Medison Co., Ltd.2022
K220043HERA W10 Diagnostic Ultrasound System, HERA W9 Diagnostic U...Samsung Medison Co., Ltd.2022
K210068HS50 Diagnostic Ultrasound System, HS60 Diagnostic Ultrasou...Samsung Medison Co., Ltd.2021

Later devices that cite this one as their predicate

Devices that cite K223387
K numberDeviceApplicantYear
K242594DEEPECHODeepecho2025
K243684BrightHeart View ClassifierBrightheart2025
K233112HM70 EVO Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2023
K231772V8/H8 Diagnostic Ultrasound System, V7/H7 Diagnostic Ultras...Samsung Medison Co., Ltd.2023

Trace the full predicate network for K223387

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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