# Distronic Sterile Products, Inc.

- Location (FDA's records): Portsmouth, NH
- FDA decisions: 8 (1995–1996): 8 510(k) clearances
- Product codes: FPA (5), FPK (2), FMG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Command Medical Products: 1 (https://510kreport.com/company/command-medical-products)
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)

## Its most-cited devices
- K950597: Core-Resistant Huber Infusion Set with Y-Site (1995), cited by 2

## Recent decisions
- K955709: Winged & Subcutaneous Infusion Sets (Feb 21, 1996)
- K955732: Vented Solution Set (Feb 21, 1996)
- K954984: Minibore Stopcock Set (Jan 23, 1996)
- K954983: Extension Set with Check Valve (Jan 23, 1996)
- K952664: Solution Administration Set (Aug 7, 1995)
- K950597: Core-Resistant Huber Infusion Set with Y-Site (Jul 26, 1995)
- K952663: 60 Micro Volume Extension Set W/.22 Micron Filter, 21 Extension Set W/1.2 Mivton Gilyrt, Inj. Site, Clamp (Jul 14, 1995)
- K945184: Intravascular Administration Set (Feb 8, 1995)

Source page: https://510kreport.com/company/distronic-sterile-products