Sensatronix Medical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sensatronix Medical Systems, Inc. makes
Sensatronix Medical Systems, Inc. manufactures nasogastric PH suction catheters, such as the ST-5001 model, and PH monitoring systems designed for clinical use.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Nasogastric Ph Suction Catheter, St-5001 Ref K891410
Regimes: 510(k) Registry: 510(k)Ph Monitoring System Ref K872929
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensatronix Medical Systems, Inc. have in the registry?
The registry currently lists 2 devices for Sensatronix Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensatronix Medical Systems, Inc.'s devices?
Among its 2 most recently registered devices, Sensatronix Medical Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sensatronix Medical Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sensatronix Medical Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sensatronix Medical Systems, Inc. in the registry?
The most recently registered devices listed for Sensatronix Medical Systems, Inc. include NASOGASTRIC PH SUCTION CATHETER, ST-5001 and PH MONITORING SYSTEM.