Gorman Rupp Industries - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Gorman Rupp Industries has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1976 to 1977. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Gorman Rupp Industries Filter by specialty or product code using the sidebar.
6 devices
Cleared
Sep 06, 1977
AQUAMATIC K-MODULE MODEL K-20
Cardiovascular
26d
Cleared
Jun 08, 1977
AQUAMATIC K-77
Cardiovascular
30d
Cleared
Feb 14, 1977
BLOOD/FLUID WARMER MODEL DW-1000A
Hematology
7d
Cleared
Jan 10, 1977
AQUAMATIC K-MODULE MODEL K-10
Pathology
14d
Cleared
Dec 16, 1976
DISPOSABLE K-PADS
Physical Medicine
50d
Cleared
Dec 06, 1976
ELECTRONIC CONTROL UNIT
Cardiovascular
14d