Gorman Rupp Industries

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K771537AQUAMATIC K-MODULE MODEL K-20September 6, 1977
K770839AQUAMATIC K-77June 8, 1977
K770232BLOOD/FLUID WARMER MODEL DW-1000AFebruary 14, 1977
K761337AQUAMATIC K-MODULE MODEL K-10January 10, 1977
K760910DISPOSABLE K-PADSDecember 16, 1976
K761087ELECTRONIC CONTROL UNITDecember 6, 1976