Fluidotherapy Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Fluidotherapy Corp. makes
Fluidotherapy Corp. manufactures ultrasound therapy equipment, including the SONOPULS 434, and electromyography (EMG) systems with temperature monitoring, such as the ENRAF NONIVS2. Their portfolio also includes the CURAMED 402, a device used for therapeutic applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the US. The company operates from the United States.
Catalogue
Sonopuls 434 Ultrasound Therapy Equipment Ref K850640
Regimes: 510(k) Registry: 510(k)Enraf NONIVS2 Channel Emg/Temp. Feed Ref K832122
Regimes: 510(k) Registry: 510(k)Curamed 402 Ref K850573
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fluidotherapy Corp. have in the registry?
The registry currently lists 3 devices for Fluidotherapy Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fluidotherapy Corp.'s devices?
Among its 3 most recently registered devices, Fluidotherapy Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Fluidotherapy Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Fluidotherapy Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fluidotherapy Corp. in the registry?
The most recently registered devices listed for Fluidotherapy Corp. include SONOPULS 434 ULTRASOUND THERAPY EQUIPMENT, ENRAF NONIVS2 CHANNEL EMG/TEMP. FEED and CURAMED 402.