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FDA 510(k)

CEREGLIDE 92 Catheter System

K-Number: K233982 · 2024-05-09

ApplicantCerenovus, Inc.
Decision Date2024-05-09
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CEREGLIDE 92 Catheter System is a medical device manufactured by Cerenovus, Inc.. It received FDA 510(k) clearance on 2024-05-09 under approval number K233982. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREGLIDE 92 Catheter System?

CEREGLIDE 92 Catheter System is a medical device that received FDA 510(k) clearance on 2024-05-09. It is manufactured by Cerenovus, Inc.. The 510(k) number is K233982.

When was CEREGLIDE 92 Catheter System approved by the FDA?

CEREGLIDE 92 Catheter System received FDA 510(k) clearance on 2024-05-09, under approval number K233982.

What company makes CEREGLIDE 92 Catheter System?

CEREGLIDE 92 Catheter System is manufactured by Cerenovus, Inc..

What is the FDA product code for CEREGLIDE 92 Catheter System?

The FDA product code for CEREGLIDE 92 Catheter System is QJP.

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Other Devices by Cerenovus, Inc.

K230726CEREGLIDE 92 Intermediate Catheter K221930CEREGLIDE 71 Intermediate Catheter K221934CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set K241244CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter K241221CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set K233988Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set

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Related Devices (Code: QJP)

K203043Route 92 Medical 070 Access SystemRoute 92 Medical, Inc. K201682RIST Radial Access CatheterRist Neurovascular, Inc. K201518Route 92 Medical 088 Access SystemRoute 92 Medical K201076Anchor Dual Lumen Guidewire CatheterAqure Medical, Inc. K200910BOSS Balloon Guide CatheterMarblehead Medical K200417RIST Radial Access CatheterRist Neurovascular, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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