System Analysis Corp.
FranceFDA 510(k) applicant, unverified
- Devices
- 1
What System Analysis Corp. makes
System Analysis Corp. manufactures the SPIROTEQ, a device designed for respiratory function assessment, likely used in clinical or diagnostic settings to measure spirometry parameters such as lung volume and airflow.
The SPIROTEQ is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Spiroteq Ref K894556
510(k) 510(k)
Frequently asked questions
How many devices does System Analysis Corp. have in the registry?
The registry currently lists 1 device for System Analysis Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list System Analysis Corp.'s devices?
Among its 1 most recently registered device, System Analysis Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do System Analysis Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for System Analysis Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from System Analysis Corp. in the registry?
The most recently registered devices listed for System Analysis Corp. include SPIROTEQ.