Psitron
Country not established
- Devices
- 2
What Psitron makes
Psitron manufactures physiological pressure transducers, including the PCM3630 model, designed for measuring and monitoring blood pressure or other fluid pressures in clinical settings.
The company’s portfolio is regulated under Class II devices in the US, with products listed via the FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Stimulator, Nerve, Transcutaneous Ref K781277
Regimes: 510(k) Registry: 510(k)Physiological Press. Transducer PCM3630 Ref K823334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Psitron have in the registry?
The registry currently lists 2 devices for Psitron. Devices recorded under merged duplicate company entries are counted once.
Which registries list Psitron's devices?
Among its 2 most recently registered devices, Psitron has devices listed in FDA 510(k) (2 devices).
What risk classes do Psitron's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Psitron's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Psitron in the registry?
The most recently registered devices listed for Psitron include STIMULATOR, NERVE, TRANSCUTANEOUS and PHYSIOLOGICAL PRESS. TRANSDUCER PCM3630.