Medical Device Manufacturer · US , Rochester , NY

Rabar, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1982

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Rabar, Inc. Neurology ✕

2 devices

1-2 of 2

Cleared Jul 27, 1984

ECHO PULSE BURST

Neurology · 38d

Cleared Dec 09, 1982

ECHO-PULSE KM555

Neurology · 178d