Cussionair Therapy Products, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Cussionair Therapy Products, Inc. makes
Cussionair Therapy Products, Inc. manufactures percussive therapy devices, including the MJ Neonatal Percussor and MJ Percussor, designed to assist in respiratory care for patients, particularly neonates and pediatric populations.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mj Neonatal Percussor Ref K812151
510(k) 510(k)Mj Percussor Ref K800713
510(k) 510(k)
Frequently asked questions
How many devices does Cussionair Therapy Products, Inc. have in the registry?
The registry currently lists 2 devices for Cussionair Therapy Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cussionair Therapy Products, Inc.'s devices?
Among its 2 most recently registered devices, Cussionair Therapy Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cussionair Therapy Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cussionair Therapy Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cussionair Therapy Products, Inc. in the registry?
The most recently registered devices listed for Cussionair Therapy Products, Inc. include MJ NEONATAL PERCUSSOR and MJ PERCUSSOR.