Piper Access, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210047Stiletto Extended Dwell CatheterAugust 27, 2021
K191976Piper GO-IO Intraosseous Infusion SystemNovember 13, 2019
K1819045 FR Dual Lumen Piper PICCSeptember 25, 2018