The Buddy Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What The Buddy Systems, Inc. makes
The Buddy Systems, Inc. manufactures health information systems, including standalone units and versions equipped with optional ECG electrodes for monitoring vital signs.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
The Buddy System/Health Information System Ref K864318
Regimes: 510(k) Registry: 510(k)The Buddy System W/Optional Ecg Electrode Ref K871748
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Buddy Systems, Inc. have in the registry?
The registry currently lists 2 devices for The Buddy Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Buddy Systems, Inc.'s devices?
Among its 2 most recently registered devices, The Buddy Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Buddy Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Buddy Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Buddy Systems, Inc. in the registry?
The most recently registered devices listed for The Buddy Systems, Inc. include THE BUDDY SYSTEM/HEALTH INFORMATION SYSTEM and THE BUDDY SYSTEM W/OPTIONAL ECG ELECTRODE.