Medapps, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Medapps, Inc. makes
Medapps, Inc. manufactures remote patient monitoring systems, including the Medapps 2.0 Remote Patient Monitoring System and the Model MA 100. These devices are designed to collect and transmit vital signs and health data from patients in outpatient or home settings to healthcare providers for real-time or delayed assessment.
The company’s remote monitoring systems fall under Class II regulatory classification in the US and are listed via 510(k) clearance with the FDA. The devices are intended for use within the United States.
Catalogue
Medapps 2.0 Remote Patient Monitoring System Ref K083862
Regimes: 510(k) Registry: 510(k)Medapps Remote Patient Monitoring, Model Ma 100 Ref K062377
Regimes: 510(k) Registry: 510(k)Medapps 2.0 Remote Patient Monitoring System Ref K112559
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medapps, Inc. have in the registry?
The registry currently lists 3 devices for Medapps, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medapps, Inc.'s devices?
Among its 3 most recently registered devices, Medapps, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Medapps, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medapps, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medapps, Inc. in the registry?
The most recently registered devices listed for Medapps, Inc. include MEDAPPS 2.0 REMOTE PATIENT MONITORING SYSTEM and MEDAPPS REMOTE PATIENT MONITORING, MODEL MA 100.