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Piper Access, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K210047
Stiletto Extended Dwell Catheter
August 27, 2021
K191976
Piper GO-IO Intraosseous Infusion System
November 13, 2019
K181904
5 FR Dual Lumen Piper PICC
September 25, 2018