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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 the device name listed in this FDA 510(k) record. The listed applicant is Cerenovus, Inc.. It received FDA 510(k) clearance on 2024-05-09 under 510(k) 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. The listed applicant is Cerenovus, Inc.. The 510(k) number is K233982.

When did CEREGLIDE 92 Catheter System receive FDA 510(k) clearance?

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

Who is the listed applicant for CEREGLIDE 92 Catheter System?

The FDA 510(k) record lists Cerenovus, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Cerenovus, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262419MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730); MICRUSFRAME (MFR100816); MICRUSFRAME (MFR100829); MICRUSFRAME (MFR140225); MICRUSFRAME (MFR140303); MICRUSFRAME (MFR140304); MICRUSFRAME (MFR140306); MICRUSFRAME (MFR140406); MICRUSFRAME (MFK262398CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing setPMA P990040tissue adhesive for use in embolization of brain arteriovenous malformationsK251828CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing SetK241244CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate CatheterK241221CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set

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Related Devices (Code: QJP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260199SLIM MicrocatheterBalt USA, LLCK253901Millipede88 Access CatheterPerfuze, Ltd.K261889Trevo Trak 21 MicrocatheterStryker NeurovascularK261808ISAAC Neurovascular Navigation CatheterMicrovention Inc. d/b/a Terumo NeuroK261549BOBBY Balloon Guide CatheterMicroVention, Inc., d/b/a Terumo NeuroK253359Zenith Distal Access Long SheathSuzhou Zenith Vascular SciTech Limited

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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