Thermowave Medical Device Corp.
Country not established
- Devices
- 1
What Thermowave Medical Device Corp. makes
Thermowave Medical Device Corp. manufactures the PulsAir Model SP-1, a portable device designed for respiratory therapy, likely delivering aerosolized medication or humidification to patients.
The company’s portfolio is regulated under FDA’s Class I device classification, with the PulsAir Model SP-1 listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Pulsair Model Sp-1 Ref K832177
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thermowave Medical Device Corp. have in the registry?
The registry currently lists 1 device for Thermowave Medical Device Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thermowave Medical Device Corp.'s devices?
Among its 1 most recently registered device, Thermowave Medical Device Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Thermowave Medical Device Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Thermowave Medical Device Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Thermowave Medical Device Corp. in the registry?
The most recently registered devices listed for Thermowave Medical Device Corp. include PULSAIR MODEL SP-1.