Research Medical, Inc. - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
Research Medical, Inc. has 35 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 35 cleared submissions from 1984 to 1997.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Research Medical, Inc.
35 devices
Cleared
Jul 08, 1997
RMI HEMOCONCENTRATOR PREFERENCE PACK
Gastroenterology & Urology
130d
Cleared
Feb 19, 1997
RMI DUAL FLUID IRRIGATING SYRINGE
General Hospital
79d
Cleared
Aug 13, 1996
RMI HEMOCONCENTRACTOR TUBING SET
Cardiovascular
88d
Cleared
Mar 26, 1996
RMI INTERNAL MAMMARY ARTERY CANNULA
Cardiovascular
75d
Cleared
Aug 15, 1995
RMI HEMOCONCENTRATOR
Gastroenterology & Urology
144d
Cleared
Jan 29, 1993
RMI SURGICCAL SITE VISUALIZATION WAND
General Hospital
270d
Cleared
Dec 18, 1992
RMI EXTERNAL CORONARY ARTERY OCCLUDER
Cardiovascular
294d
Cleared
Dec 08, 1992
RMI NORMOCLUDER CORONARY ARTERY OCCLUDER
Cardiovascular
343d
Cleared
Apr 15, 1992
RMI SOFCLAMP
Cardiovascular
61d
Cleared
May 16, 1991
RMI VASCULAR TOURNIQUET KIT
Cardiovascular
119d
Cleared
Jun 08, 1990
RMI CARDIOPLEGIA DELIVERY KITS
Cardiovascular
86d
Cleared
Mar 27, 1990
RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORING
Cardiovascular
90d