Amplife Corporation
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Amplife Corporation makes
Amplife Corporation manufactures digital infrared ear thermometers, including the Model E101, and wrist and upper arm blood pressure monitors (Models M600 and M100). The company also produces digital clinical thermometers designed for medical use.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Amplief Wrist Blood Pressure Monitor, Model M600 Ref K050413
510(k) 510(k)- 510(k) 510(k)
Amplife Digital Clinical Thermometer Ref K042575
510(k) 510(k)
Frequently asked questions
How many devices does Amplife Corporation have in the registry?
The registry currently lists 4 devices for Amplife Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amplife Corporation's devices?
Among its 4 most recently registered devices, Amplife Corporation has devices listed in FDA 510(k) (4 devices).
What risk classes do Amplife Corporation's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Amplife Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amplife Corporation in the registry?
The most recently registered devices listed for Amplife Corporation include AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101, AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600, AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100 and AMPLIFE DIGITAL CLINICAL THERMOMETER.