Class Class II
Arrow® Nitinol Wire (K241784)
Description
Arrow® Nitinol Wire by Teleflex Medical, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241784
Clearance Date2024-09-18
Clearance TypeTraditional
Product CodeDQX
Regulation Number870.1330
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241784
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Arrow® Nitinol Wire (K241784) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K142393 | PREDICATE III GUIDEWIRE | Lake Region Medical | 2014 |
Trace the full predicate network for K241784
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.