Rabar, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Rabar, Inc. makes
Rabar, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the MICROTENS 7757 T.E.N.S. STIMULATOR, and ultrasound therapy units such as the ECHO-PULSE KM555 and ECHO PULSE BURST for localized tissue treatment.
These devices are classified as Class I and Class II under FDA regulations, with some models supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Microtens 7757 T.E.N.S. Stimulator Ref K844017
Regimes: 510(k) Registry: 510(k)Echo-Pulse KM555 Ref K821736
Regimes: 510(k) Registry: 510(k)Echo Pulse Burst Ref K842414
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rabar, Inc. have in the registry?
The registry currently lists 3 devices for Rabar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rabar, Inc.'s devices?
Among its 3 most recently registered devices, Rabar, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Rabar, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Rabar, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rabar, Inc. in the registry?
The most recently registered devices listed for Rabar, Inc. include MICROTENS 7757 T.E.N.S. STIMULATOR, ECHO-PULSE KM555 and ECHO PULSE BURST.