Arvee Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Arvee Medical, Inc. makes
Arvee Medical, Inc. manufactures apnea monitors for infants and adults, including the ARVEE Apnea Monitor (Models 2400 and 4800) and an Infant Monitor (Model 2400). These devices are designed to detect and alert users to breathing interruptions, such as apnea events, in pediatric and adult patients.
The company’s portfolio consists of Class II medical devices, all of which are listed under the FDA’s 510(k) clearance process. These products are intended for use in the United States, where regulatory compliance is managed through the FDA’s device classification system.
Catalogue
Arvee Apnea Monitor, Model 2400 Ref K891676
Regimes: 510(k) Registry: 510(k)Infant Monitor, Model 2400 Ref K872631
Regimes: 510(k) Registry: 510(k)Arvee Apnea Monitor, Model 4800 Ref K900730
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arvee Medical, Inc. have in the registry?
The registry currently lists 3 devices for Arvee Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arvee Medical, Inc.'s devices?
Among its 3 most recently registered devices, Arvee Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Arvee Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Arvee Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arvee Medical, Inc. in the registry?
The most recently registered devices listed for Arvee Medical, Inc. include ARVEE APNEA MONITOR, MODEL 2400, INFANT MONITOR, MODEL 2400 and ARVEE APNEA MONITOR, MODEL 4800.