# Piper Access, LLC

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 3 (2018–2021): 3 510(k) clearances
- Product codes: FMI (1), PND (1), LJS (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 2 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)
- Vidacare Corporation: 1 (https://510kreport.com/company/vidacare)

## Firms that cite its devices most
- Bard Access Systems, Inc (Bas)[Wholly-Owned Subsidiary of Bd]: 1 (https://510kreport.com/company/bard-access-systems-bas-wholly-owned-subsidiary-of-bd)

## Its most-cited devices
- K191976: Piper GO-IO Intraosseous Infusion System (2019), cited by 1

## Recent decisions
- K210047: Stiletto Extended Dwell Catheter (Aug 27, 2021)
- K191976: Piper GO-IO Intraosseous Infusion System (Nov 13, 2019)
- K181904: 5 FR Dual Lumen Piper PICC (Sep 25, 2018)

Source page: https://510kreport.com/company/piper-access