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FDA 510(k)

Zipline Access Catheter

K-Number: K240711 · 2024-10-17

ApplicantPerfuze, Ltd.
Decision Date2024-10-17
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Zipline Access Catheter is a medical device manufactured by Perfuze, Ltd.. It received FDA 510(k) clearance on 2024-10-17 under approval number K240711. 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 Zipline Access Catheter?

Zipline Access Catheter is a medical device that received FDA 510(k) clearance on 2024-10-17. It is manufactured by Perfuze, Ltd.. The 510(k) number is K240711.

When was Zipline Access Catheter approved by the FDA?

Zipline Access Catheter received FDA 510(k) clearance on 2024-10-17, under approval number K240711.

What company makes Zipline Access Catheter?

Zipline Access Catheter is manufactured by Perfuze, Ltd..

What is the FDA product code for Zipline Access Catheter?

The FDA product code for Zipline Access Catheter is QJP.

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Official Source

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