# Dayspring Medical, Inc.

- Location (FDA's records): Boulder, CO
- FDA decisions: 5 (1996–1999): 5 510(k) clearances
- Product codes: FJI (3), FKY (1), LLB (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
- K991005: Vented Diakysate Port Ccap, Red Pliable Vinyl - Dayspring Medical Part NO, DPC101VS (Jun 22, 1999)
- K991003: Pump Segment Rinse Line W/ Slip-on Connector, Pump Segment Rinse Line W/ Luer-Lock Connector, T-Connector, Short, W/ Sli (Jun 9, 1999)
- K961039: Bllod Port Cap, Dialysate Port Cap, Vented Dialysate Port Cap with Red Pliable Vinyl (Sep 12, 1996)
- K961040: Blood Port Cap, Dialysate Port Cap, Red Hard Plastic (Jun 11, 1996)
- K961026: Blood Port Cap, Luer-Lock Fitting, Dayspring Medical Part NO. BPC252LL (Jun 10, 1996)

Source page: https://510kreport.com/company/dayspring-medical