Medical Device Manufacturer · US , Mchenry , IL

Gorman Rupp Industries - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1976

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Gorman Rupp Industries Cardiovascular ✕

3 devices

1-3 of 3

Cleared Sep 06, 1977

AQUAMATIC K-MODULE MODEL K-20

Cardiovascular · 26d

Cleared Jun 08, 1977

Cardiovascular · 30d

Cleared Dec 06, 1976

ELECTRONIC CONTROL UNIT

Cardiovascular · 14d