# Pulse Scientific, Inc.

- Location (FDA's records): Burlington, Ont., Canada, CA
- FDA decisions: 3 (1992–1992): 3 510(k) clearances
- Product codes: KTN (1), DHR (1), DCK (1)
- 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
- K923768: Pulse CRP Test (Dec 1, 1992)
- K923767: Pulse IM Red Cell Test (Oct 16, 1992)
- K923771: Pulse RF Test (Oct 5, 1992)

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