# Pulse Metric, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 5 (1991–2002): 5 510(k) clearances
- Product codes: DXN (5)
- 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
- Ostar Meditech Corp.: 1 (https://510kreport.com/company/ostar-meditech)

## Its most-cited devices
- K012498: Dynapulse 500G (DP500G) Bllod Pressure Monitoring System (2001), cited by 1

## Recent decisions
- K013478: Dynapulse 5200A Pathway Blood Pressure Monitoring System (Jan 10, 2002)
- K013358: Dynapulse 5000A Mini Abp Blood Pressure Monitoring System (Dec 13, 2001)
- K012498: Dynapulse 500G (DP500G) Bllod Pressure Monitoring System (Nov 1, 2001)
- K945111: Dynapulse 5000A (DP5000A) (Jun 23, 1995)
- K904739: Dynapulse 200M (Jan 8, 1991)

Source page: https://510kreport.com/company/pulse-metric