Class Class II

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter (K241244)

K241244 2024-10-16 Traditional
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Description

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter by Cerenovus, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241244
Clearance Date2024-10-16
Clearance TypeTraditional
Product CodeQJP
Regulation Number870.1250

Categories

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Predicate lineage for K241244

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. CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter (K241244) 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
K202752AXS Vecta 46 Intermediate CatheterStryker Neurovascular2021

Trace the full predicate network for K241244

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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