# Pulse Time Products, Ltd.

- Location (FDA's records): Chichester, W. Sussex, GB
- FDA decisions: 6 (1981–1990): 6 510(k) clearances
- Product codes: DRT (4), DXN (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K901392: BP50 Blood Pressure and Pulse Monitor (Aug 23, 1990)
- K892795: Pulse Time Products Limited, PM-3 (Aug 25, 1989)
- K892794: Pulse Time Products Limited, PM-2 (Aug 25, 1989)
- K864411: Pulse/B.P. Monitor (Jun 24, 1987)
- K864748: PM-8 Heart Rate Monitor (Mar 20, 1987)
- K811425: Cardiacmonitors (Sep 16, 1981)

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