# Amplife Corporation

- Location (FDA's records): Great Neck, NY
- FDA decisions: 4 (2004–2005): 4 510(k) clearances
- Product codes: FLL (2), DXN (2)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Microlife Intellectual Property GmbH: 1 (https://510kreport.com/company/microlife-intellectual-property)
- Microlife Intellectual Property Gmb: 1 (https://510kreport.com/company/microlife-intellectual-property-gmb)

## Recent decisions
- K050413: Amplief Wrist Blood Pressure Monitor, Model M600 (Mar 4, 2005)
- K043550: Amplife Upper Arm Blood Pressure Monitor, Model M100 (Jan 27, 2005)
- K042906: Amplife Digital Infrared Ear Thermometer, Model E101 (Nov 19, 2004)
- K042575: Amplife Digital Clinical Thermometer (Sep 30, 2004)

Source page: https://510kreport.com/company/amplife