Chest M.I., Inc.
Country not established
- Devices
- 2
What Chest M.I., Inc. makes
Chest M.I., Inc. manufactures spirometry systems, including the CARDIOTECH GT-105 and the SPIRO-MASTER PC-10, designed for pulmonary function testing and lung volume measurement.
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
Cardiotech Spirometry System, Model Gt-105 Ref K090646
Regimes: 510(k) Registry: 510(k)Spiro-Master Pc-10 Spirometry System Ref K080921
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chest M.I., Inc. have in the registry?
The registry currently lists 2 devices for Chest M.I., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chest M.I., Inc.'s devices?
Among its 2 most recently registered devices, Chest M.I., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Chest M.I., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Chest M.I., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chest M.I., Inc. in the registry?
The most recently registered devices listed for Chest M.I., Inc. include CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105 and SPIRO-MASTER PC-10 SPIROMETRY SYSTEM.