Linshom Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Linshom Medical, Inc. makes
Linshom Medical, Inc. manufactures the Continuous Predictive Respiratory Monitoring System (CPRMS), a device designed for continuous monitoring of respiratory function to predict and alert on potential respiratory events in patients.
The CPRMS 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
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Linshom Medical, Inc. have in the registry?
The registry currently lists 2 devices for Linshom Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Linshom Medical, Inc.'s devices?
Among its 2 most recently registered devices, Linshom Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Linshom Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Linshom Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Linshom Medical, Inc. in the registry?
The most recently registered devices listed for Linshom Medical, Inc. include Linshom Continuous Predictive Respiratory Monitoring System (CPRMS).