Multispiro, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Multispiro, Inc. makes
Multispiro, Inc. manufactures respiratory devices, including the Multispiro-Breeze, a portable inhaler system, and The Peak, a peak flow meter for monitoring lung function. The Multispiro-SX is a single-use inhaler designed for controlled medication delivery.
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
Multispiro-Breeze Ref K913681
Regimes: 510(k) Registry: 510(k)The Peak Ref K920390
Regimes: 510(k) Registry: 510(k)Multispiro-Sx Ref K915451
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Multispiro, Inc. have in the registry?
The registry currently lists 3 devices for Multispiro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Multispiro, Inc.'s devices?
Among its 3 most recently registered devices, Multispiro, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Multispiro, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Multispiro, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Multispiro, Inc. in the registry?
The most recently registered devices listed for Multispiro, Inc. include MULTISPIRO-BREEZE, THE PEAK and MULTISPIRO-SX.