Piper Access, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Piper Access, LLC - FDA 510(k) Cleared Devices
Recent clearances: Stiletto Extended Dwell Catheter, Piper GO-IO Intraosseous Infusion System, 5 FR Dual Lumen Piper PICC
3
Total
3
Cleared
0
Denied
Piper Access, LLC has 3 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Last cleared in 2021. Active since 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Piper Access, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Piper Access, LLC
3 devices