Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
Arrow International, Inc. (Subsidiary of Teleflex, Inc.) appears in FDA public data with 0 recalls, 8 510(k) clearances, 12 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 9, 2018.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 12
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K180395 | EZ-IO Intraosseous Vascular Access System | November 9, 2018 |
| K163513 | Arrow Endurance Extended Dwell Peripheral Catheter System | February 24, 2017 |
| K161313 | ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and Antithrombogenic Techn | August 24, 2016 |
| K160018 | Arrow Quickflash Arterial Catheterization Device | June 13, 2016 |
| K153487 | CG+ Arrow PICC powered by Arrow VPS Stylet PLUS and Arrow VPS Stylet PLUS | February 4, 2016 |
| K153423 | CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC | January 28, 2016 |
| K152272 | Arrow Endurance Extended Dwell Peripheral Catheter System | November 23, 2015 |
| K143102 | Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions | July 24, 2015 |