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FDA 510(k)

CEREGLIDE 71 Intermediate Catheter

K-Number: K221930 · 2023-03-09

ApplicantCerenovus, Inc.
Decision Date2023-03-09
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CEREGLIDE 71 Intermediate Catheter is a medical device manufactured by Cerenovus, Inc.. It received FDA 510(k) clearance on 2023-03-09 under approval number K221930. 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 71 Intermediate Catheter?

CEREGLIDE 71 Intermediate Catheter is a medical device that received FDA 510(k) clearance on 2023-03-09. It is manufactured by Cerenovus, Inc.. The 510(k) number is K221930.

When was CEREGLIDE 71 Intermediate Catheter approved by the FDA?

CEREGLIDE 71 Intermediate Catheter received FDA 510(k) clearance on 2023-03-09, under approval number K221930.

What company makes CEREGLIDE 71 Intermediate Catheter?

CEREGLIDE 71 Intermediate Catheter is manufactured by Cerenovus, Inc..

What is the FDA product code for CEREGLIDE 71 Intermediate Catheter?

The FDA product code for CEREGLIDE 71 Intermediate Catheter is QJP.

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Other Devices by Cerenovus, Inc.

K230726CEREGLIDE 92 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 K233982CEREGLIDE 92 Catheter System K233988Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set

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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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