Phycon
Country not established
- Devices
- 2
What Phycon makes
Phycon manufactures disposable hydrogel-based external pacing and defibrillation electrodes, designed for temporary cardiac rhythm management and resuscitation procedures. These include external pacing and defibrillation electrodes intended for use in emergency and clinical settings where temporary cardiac support is required.
The company’s products fall under Class II medical devices in the US and are listed in the FDA 510(k) registry. These devices are regulated under the US Food and Drug Administration’s authority, ensuring compliance with performance and safety standards for temporary cardiac intervention technologies.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phycon have in the registry?
The registry currently lists 2 devices for Phycon. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phycon's devices?
Among its 2 most recently registered devices, Phycon has devices listed in FDA 510(k) (2 devices).
What risk classes do Phycon's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Phycon's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Phycon in the registry?
The most recently registered devices listed for Phycon include DISP. POLYMER (HYDROGEL) EXTERNAL PACING & DEFIB. and DISP. GEL EXTERNAL PACING & DEFIBRILLATION ELECT..