Bow/Parm
Country not established
- Devices
- 1
What Bow/Parm makes
Bow/Parm manufactures a hypothermia oxygen warmer-treatment system designed to regulate and deliver warmed oxygen during therapeutic hypothermia procedures, ensuring patient temperature control in critical care settings.
The company’s hypothermia oxygen warmer-treatment system is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The product is based in the United States.
Catalogue
Hypothermia Oxygen Warmer-Treatment Sys Ref K841295
510(k) 510(k)
Frequently asked questions
How many devices does Bow/Parm have in the registry?
The registry currently lists 1 device for Bow/Parm. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bow/Parm's devices?
Among its 1 most recently registered device, Bow/Parm has devices listed in FDA 510(k) (1 device).
What risk classes do Bow/Parm's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bow/Parm's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bow/Parm in the registry?
The most recently registered devices listed for Bow/Parm include HYPOTHERMIA OXYGEN WARMER-TREATMENT SYS.