Spirosure, Inc.
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- Devices
- 1
What Spirosure, Inc. makes
Spirosure, Inc. manufactures the Fenom Pro Nitric Oxide Test, a device used for measuring exhaled nitric oxide levels in patients to assess airway inflammation or respiratory conditions.
The company’s products are regulated as Class II medical devices in the United States and are listed under the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Fenom Pro Nitric Oxide Test Ref K182874
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spirosure, Inc. have in the registry?
The registry currently lists 1 device for Spirosure, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spirosure, Inc.'s devices?
Among its 1 most recently registered device, Spirosure, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Spirosure, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Spirosure, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spirosure, Inc. in the registry?
The most recently registered devices listed for Spirosure, Inc. include Fenom Pro Nitric Oxide Test.