# Lifestream Technologies, Inc.

- Location (FDA's records): Post Falls, ID
- FDA decisions: 3 (1999–2004): 3 510(k) clearances
- Product codes: CHH (2), NFX (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
- K033899: Lifestream Plus Cholesterol Monitor, Modification to Resolution Cholesterol Monitor (May 20, 2004)
- K000610: Resolution Cholesterol Monitor (Jul 21, 2000)
- K993096: Privalink Software Accessory to the Lifestream Cholesterol Monitor (Dec 20, 1999)

Source page: https://510kreport.com/company/lifestream-technologies