# Medwave, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 5 (1995–2006): 5 510(k) clearances
- Product codes: DXN (5)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K011152: Vasotrac APM205A (2001), cited by 1
- K001898: Vasotrax (2000), cited by 1

## Recent decisions
- K061557: Fusion (Sep 15, 2006)
- K053185: Primo Noninvasive Blood Pressure Measurement System (Jan 24, 2006)
- K011152: Vasotrac APM205A (May 31, 2001)
- K001898: Vasotrax (Aug 31, 2000)
- K950249: Vasotrac Blood Pressure Monitor, Model - Apm 205 (Feb 1, 1995)

Source page: https://510kreport.com/company/medwave