Fellmar Company
Country not established
- Devices
- 1
What Fellmar Company makes
Fellmar Company manufactures snorkels designed for respiratory support and airway management, intended for use in medical or clinical settings.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is registered in the United States.
Catalogue
Snorkel Ref K112766
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fellmar Company have in the registry?
The registry currently lists 1 device for Fellmar Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fellmar Company's devices?
Among its 1 most recently registered device, Fellmar Company has devices listed in FDA 510(k) (1 device).
What risk classes do Fellmar Company's devices fall under?
Among its 1 most recently registered device, the classes recorded for Fellmar Company's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fellmar Company in the registry?
The most recently registered devices listed for Fellmar Company include SNORKEL.