# Bd/Preefil

- Location (FDA's records): Franklin Lakes, NJ
- FDA decisions: 1 (2000–2000): 1 510(k) clearance
- Product codes: FOZ (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- Vital Signs, Inc.: 1 (https://510kreport.com/company/vital-signs)

## Firms that cite its devices most
- Bd: 2 (https://510kreport.com/company/bd)

## Its most-cited devices
- K982558: BD Preefile Normal Saline Flush Syringe Flush Syringe (2000), cited by 2

## Recent decisions
- K982558: BD Preefile Normal Saline Flush Syringe Flush Syringe (Mar 8, 2000)

Source page: https://510kreport.com/company/bd-preefil