Company · US
Arrow International, LLC (A subsidiary of Teleflex, Inc.)
FDA 510(k) clearances and medical device recalls filed under this name, 2015 to 2025. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 14, 2025 | K243599 | Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00818) Arrow International, LLC (A subsidiary of Teleflex, Inc.) | FOZ |
| Dec 20, 2024 | K242281 | Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended Dwell Peripheral Cathete Arrow International, LLC (A subsidiary of Teleflex, Inc.) | FOZ |
| Aug 30, 2022 | K220280 | Arrow Stiffening Stylet Arrow International, LLC (A subsidiary of Teleflex, Inc.) | DRB |
| Aug 22, 2022 | K220363 | VPS Rhythm DLX Device with TipTracker Technology Arrow International, LLC (A subsidiary of Teleflex, Inc.) | LJS |
| Dec 22, 2016 | K160925 | VPS Rhythm Device with TipTracker Technology Arrow International, Inc. (A Subsidiary of Teleflex, Inc.) | LJS |
| Jun 5, 2015 | K150109 | Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter (JACC) with Sustain Technology Arrow International (A Subsidiary of Teleflex, Inc.) | FOZ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||