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FDA 510(k)

Arrow® Nitinol Wire

K-Number: K241784 · 2024-09-18

ApplicantTeleflex Medical
Decision Date2024-09-18
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Arrow® Nitinol Wire is a medical device manufactured by Teleflex Medical. It received FDA 510(k) clearance on 2024-09-18 under approval number K241784. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arrow® Nitinol Wire?

Arrow® Nitinol Wire is a medical device that received FDA 510(k) clearance on 2024-09-18. It is manufactured by Teleflex Medical. The 510(k) number is K241784.

When was Arrow® Nitinol Wire approved by the FDA?

Arrow® Nitinol Wire received FDA 510(k) clearance on 2024-09-18, under approval number K241784.

What company makes Arrow® Nitinol Wire?

Arrow® Nitinol Wire is manufactured by Teleflex Medical.

What is the FDA product code for Arrow® Nitinol Wire?

The FDA product code for Arrow® Nitinol Wire is DQX.

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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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