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 Pathology ✕

1 devices

1-1 of 1

Cleared Jan 10, 1977

AQUAMATIC K-MODULE MODEL K-10

Pathology · 14d