Research Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
35
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K970739RMI HEMOCONCENTRATOR PREFERENCE PACKJuly 8, 1997
K964833RMI DUAL FLUID IRRIGATING SYRINGEFebruary 19, 1997
K961927RMI HEMOCONCENTRACTOR TUBING SETAugust 13, 1996
K960098RMI INTERNAL MAMMARY ARTERY CANNULAMarch 26, 1996
K951344RMI HEMOCONCENTRATORAugust 15, 1995
K922083RMI SURGICCAL SITE VISUALIZATION WANDJanuary 29, 1993
K920936RMI EXTERNAL CORONARY ARTERY OCCLUDERDecember 18, 1992
K915869RMI NORMOCLUDER CORONARY ARTERY OCCLUDERDecember 8, 1992
K920676RMI SOFCLAMPApril 15, 1992
K910221RMI VASCULAR TOURNIQUET KITMay 16, 1991
K901231RMI CARDIOPLEGIA DELIVERY KITSJune 8, 1990
K897137RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORINGMarch 27, 1990
K896777RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINEFebruary 27, 1990
K896778RMI VASOPLEGIA CANNULA WITH & WITHOUT CHECK VALVEFebruary 27, 1990
K896636RMI ANTEPLEGIA CANNULAFebruary 15, 1990
K892377RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SETDecember 7, 1989
K892368RMI CARDIOPLEGIA DELIVERY SETSDecember 7, 1989
K891576FEM-FLEX FEMORAL ACCESS CANNULATION SETOctober 12, 1989
K894243RMI ARTERIAL PERFUSION CANNULASeptember 19, 1989
K880103CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.March 22, 1988