Class Class II

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) (K250592)

K250592 2025-05-12 Traditional
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Description

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) by Northeast Scientific, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250592
Clearance Date2025-05-12
Clearance TypeTraditional
Product CodeOWQ
Regulation Number870.1200

Categories

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Predicate lineage for K250592

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. NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) (K250592) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K150442Volcano Visions PV .018 Digital IVUS CatheterVolcano Corporation2015

Trace the full predicate network for K250592

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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