# Applied Membrane Technology, Inc.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 3 (1985–1987): 3 510(k) clearances
- Product codes: BZQ (2), NFB (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
- K870835: Adult Apnea Monitor (20), Monitor Interface (30) (Mar 27, 1987)
- K861423: Demand Oxygen Saver System (D02S) (May 16, 1986)
- K851235: Demand Oxygen Sauer DOS2 Model 10 (Apr 30, 1985)

Source page: https://510kreport.com/company/applied-membrane-technology