Alertwatch, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Alertwatch, Inc. makes
Alertwatch, Inc. manufactures medical alert devices, including the AlertWatch:OB—a wearable device for obstetric monitoring—and the AlertWatch:AC, designed for acute care patient alert systems. These products are intended to support real-time patient monitoring and communication in clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. The devices are listed in the FDA’s 510(k) registry. Alertwatch, Inc. is headquartered in the United States.
Catalogue
AlertWatch:OB Ref K173715
Regimes: 510(k) Registry: 510(k)AlertWatch: OR Ref K153335
Regimes: 510(k) Registry: 510(k)Alertwatch: Or Ref K130401
Regimes: 510(k) Registry: 510(k)AlertWatch:AC Ref K210160
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alertwatch, Inc. have in the registry?
The registry currently lists 4 devices for Alertwatch, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alertwatch, Inc.'s devices?
Among its 4 most recently registered devices, Alertwatch, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Alertwatch, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Alertwatch, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alertwatch, Inc. in the registry?
The most recently registered devices listed for Alertwatch, Inc. include AlertWatch:OB, AlertWatch: OR and AlertWatch:AC.