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FDA 510(k)

CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set

K-Number: K221934 · 2023-03-09

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

Device Summary

CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set is a medical device manufactured by Cerenovus, Inc.. It received FDA 510(k) clearance on 2023-03-09 under approval number K221934. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set?

CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set 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 K221934.

When was CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set approved by the FDA?

CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set received FDA 510(k) clearance on 2023-03-09, under approval number K221934.

What company makes CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set?

CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set is manufactured by Cerenovus, Inc..

What is the FDA product code for CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set?

The FDA product code for CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set is NRY.

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Other Devices by Cerenovus, Inc.

K230726CEREGLIDE 92 Intermediate Catheter K221930CEREGLIDE 71 Intermediate Catheter 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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Related Devices (Code: NRY)

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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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