Physio-Dyne Instrument Corp.
Country not established
- Devices
- 1
What Physio-Dyne Instrument Corp. makes
Physio-Dyne Instrument Corp. manufactures the EASI (Easy Analog Sampling Interface), a device designed for analog signal acquisition and processing in medical monitoring applications.
The EASI is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physio-Dyne Instrument Corp. have in the registry?
The registry currently lists 1 device for Physio-Dyne Instrument Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physio-Dyne Instrument Corp.'s devices?
Among its 1 most recently registered device, Physio-Dyne Instrument Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Physio-Dyne Instrument Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Physio-Dyne Instrument Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physio-Dyne Instrument Corp. in the registry?
The most recently registered devices listed for Physio-Dyne Instrument Corp. include PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE).