Class Class II

Marquee™ Disposable Core Biopsy Instrument and Instrument Kit (K250032)

K250032 2025-07-10 Special
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Description

Marquee™ Disposable Core Biopsy Instrument and Instrument Kit by Bard Peripheral Vascular, Inc., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250032
Clearance Date2025-07-10
Clearance TypeSpecial
Product CodeKNW
Regulation Number876.1075

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Predicate lineage for K250032

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. Marquee™ Disposable Core Biopsy Instrument and Instrument Kit (K250032) cites 2 predicate devices and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K171953Bard Mission Disposable Core Biopsy InstrumentBard Peripheral Vascular, Inc.2017
K133948BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(...Bard Peripheral Vascular, Inc.2014

Trace the full predicate network for K250032

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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