# Pro. Duct Health, Inc.

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: KNW (1), FMI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Neomatrix, LLC: 1 (https://510kreport.com/company/neomatrix)

## Its most-cited devices
- K000135: Pro.Duct Catheter, Model CTH03 (2000), cited by 1

## Recent decisions
- K001098: Pro.Duct Health Micro-Stylet, Model STY01 (May 18, 2000)
- K000135: Pro.Duct Catheter, Model CTH03 (Apr 10, 2000)

Source page: https://510kreport.com/company/pro-duct-health