Arrow® Nitinol Wire
K-Number: K241784 · 2024-09-18
Device Summary
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. The listed applicant is Teleflex Medical. The 510(k) number is K241784.
When did Arrow® Nitinol Wire receive FDA 510(k) clearance?
Arrow® Nitinol Wire received FDA 510(k) clearance on 2024-09-18, under 510(k) number K241784.
Who is the listed applicant for Arrow® Nitinol Wire?
The FDA 510(k) record lists Teleflex Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Arrow® Nitinol Wire?
The FDA product code for Arrow® Nitinol Wire is DQX.
Other records listing Teleflex Medical 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.
Related Devices (Code: DQX)
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.
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.