Sensormedix, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sensormedix, Inc. makes
Sensormedix, Inc. manufactures medical devices for respiratory function testing, including the SENSOCOR™ R-TEST 240 XL for lung volume and flow measurement, and the SENSOCOR™ DIASYS for spirometry and pulmonary function analysis.
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
Sensocor(Tm) R-Test 240 Xl Ref K881772
Regimes: 510(k) Registry: 510(k)Sensocor(Tm) Diasys Ref K881771
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensormedix, Inc. have in the registry?
The registry currently lists 2 devices for Sensormedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensormedix, Inc.'s devices?
Among its 2 most recently registered devices, Sensormedix, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sensormedix, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sensormedix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sensormedix, Inc. in the registry?
The most recently registered devices listed for Sensormedix, Inc. include SENSOCOR(TM) R-TEST 240 XL and SENSOCOR(TM) DIASYS.