SafeBeat Rx, Inc.
United Statesfrom the FDA registration address FDA FEI 3045323923
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What SafeBeat Rx, Inc. makes
SafeBeat Rx, Inc. manufactures the SafeBeat Rx App. This product is a software-based medical device.
The portfolio is regulated as a Class II device and is listed in the fda_510k registry. The company is based in the United States.
Catalogue
- Registry: GUDID
SafeBeat Rx App Ref K251218
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3045323923
- DUNS number
- 117717592
- Address
- 450 Sutter St Rm 1530, San Francisco, CA, 94108
Frequently asked questions
How many devices does SafeBeat Rx, Inc. have in the registry?
The registry currently lists 2 devices for SafeBeat Rx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SafeBeat Rx, Inc.'s devices?
Among its 2 most recently registered devices, SafeBeat Rx, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SafeBeat Rx, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for SafeBeat Rx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SafeBeat Rx, Inc. in the registry?
The most recently registered devices listed for SafeBeat Rx, Inc. include SafeBeat Rx App v2.1830.2223.160 and SafeBeat Rx App.