Ambulatory Monitoring, Inc.
United StatesFDA applicant, unverified FDA FEI 2430863
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Actillume Ref K894044
Regimes: 510(k) Registry: 510(k)Wrist Actigraph Ref K854030
Regimes: 510(k) Registry: 510(k)Sleep Watch Ref K251574
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2430863
- Address
- 731 SAW MILL RIVER RD., ARDSLEY, NY, 10502
- Website
- www.ambulatory-monitoring.com
- [email protected]
From the company website
Long-Term Physiological & Environmental Monitoring Systems Ambulatory Monitoring… the name says it all!
Frequently asked questions
How many devices does Ambulatory Monitoring, Inc. have in the registry?
The registry currently lists 3 devices for Ambulatory Monitoring, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ambulatory Monitoring, Inc.'s devices?
Among its 3 most recently registered devices, Ambulatory Monitoring, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ambulatory Monitoring, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ambulatory Monitoring, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ambulatory Monitoring, Inc. in the registry?
The most recently registered devices listed for Ambulatory Monitoring, Inc. include ACTILLUME, WRIST ACTIGRAPH and Sleep Watch.