Piper Access, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Piper Access, LLC makes
Piper Access, LLC manufactures central venous catheters, including a 5 French dual-lumen peripherally inserted central catheter (PICC) and an extended-dwell catheter for long-term venous access. The company also produces the Piper GO-IO, an intraosseous infusion system designed for rapid fluid and medication administration in emergency or pediatric settings.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance. The company is based in the United States.
Catalogue
5 FR Dual Lumen Piper PICC Ref K181904
Regimes: 510(k) Registry: 510(k)Piper GO-IO Intraosseous Infusion System Ref K191976
Regimes: 510(k) Registry: 510(k)Stiletto Extended Dwell Catheter Ref K210047
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Piper Access, LLC have in the registry?
The registry currently lists 3 devices for Piper Access, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Piper Access, LLC's devices?
Among its 3 most recently registered devices, Piper Access, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Piper Access, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Piper Access, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Piper Access, LLC in the registry?
The most recently registered devices listed for Piper Access, LLC include 5 FR Dual Lumen Piper PICC, Piper GO-IO Intraosseous Infusion System and Stiletto Extended Dwell Catheter.