Pneumedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Pneumedics, Inc. makes
Pneumedics, Inc. manufactures respiratory therapy equipment, including the SpiroLoop Pulmonary Exercise System, its modified versions, and the PB950 and PB960 models that combine DataLoop and SpiroLoop functionalities.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Spiroloop-Pulmonary Exercise System Ref K863087
Regimes: 510(k) Registry: 510(k)Spiroloop, Modification Ref K904633
Regimes: 510(k) Registry: 510(k)Models PB950 And PB960 Dataloop And Spiroloop Ref K894667
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pneumedics, Inc. have in the registry?
The registry currently lists 3 devices for Pneumedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneumedics, Inc.'s devices?
Among its 3 most recently registered devices, Pneumedics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Pneumedics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pneumedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneumedics, Inc. in the registry?
The most recently registered devices listed for Pneumedics, Inc. include SPIROLOOP-PULMONARY EXERCISE SYSTEM, SPIROLOOP, MODIFICATION and MODELS PB950 AND PB960 DATALOOP AND SPIROLOOP.