Gorman Rupp Industries

Gorman Rupp Industries holds 6 FDA 510(k) medical device clearances, first cleared 1976, most recent 1977.

Top product codes for Gorman Rupp Industries

Recent clearances by Gorman Rupp Industries

K771537 — AQUAMATIC K-MODULE MODEL K-20Code DWJ·1977-09-06
K770839 — AQUAMATIC K-77Code DWJ·1977-06-08
K770232 — BLOOD/FLUID WARMER MODEL DW-1000ACode BSB·1977-02-14
K761337 — AQUAMATIC K-MODULE MODEL K-10Code JRR·1977-01-10
K760910 — DISPOSABLE K-PADSCode ILO·1976-12-16
K761087 — ELECTRONIC CONTROL UNITCode DWJ·1976-12-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.