Sentronix, Inc.
Country not established
- Devices
- 1
What Sentronix, Inc. makes
Sentronix, Inc. manufactures the Model 20 Digital Pulse Rate Monitor, a device designed to measure and display heart rate data for patient monitoring purposes.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. Sentronix, Inc. is based in the United States.
Catalogue
Model 20 Digital Pulse Rate Monitor Ref K780937
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sentronix, Inc. have in the registry?
The registry currently lists 1 device for Sentronix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sentronix, Inc.'s devices?
Among its 1 most recently registered device, Sentronix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sentronix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sentronix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sentronix, Inc. in the registry?
The most recently registered devices listed for Sentronix, Inc. include MODEL 20 DIGITAL PULSE RATE MONITOR.