Iontec Corp.
Country not established
- Devices
- 1
What Iontec Corp. makes
Iontec Corp. manufactures the DRM 2300 Plethysmographic Cardiotachometer, a device used for measuring heart rate variability and respiratory patterns through plethysmographic techniques. It is designed to provide real-time cardiac and respiratory monitoring, often used in clinical and research settings to assess autonomic nervous system function.
The company’s portfolio is regulated under Class II medical devices in the United States, with the DRM 2300 Plethysmographic Cardiotachometer listed via the FDA’s 510(k) pathway. The device is intended for use within the regulatory framework of the US market.
Catalogue
Drm 2300 Plethysmographic Cardiotachometer Ref K871149
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iontec Corp. have in the registry?
The registry currently lists 1 device for Iontec Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iontec Corp.'s devices?
Among its 1 most recently registered device, Iontec Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Iontec Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Iontec Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iontec Corp. in the registry?
The most recently registered devices listed for Iontec Corp. include DRM 2300 PLETHYSMOGRAPHIC CARDIOTACHOMETER.