Research Medical, Inc.
Research Medical, Inc. appears in FDA public data with 0 recalls, 35 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 8, 1997.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 35
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K970739 | RMI HEMOCONCENTRATOR PREFERENCE PACK | July 8, 1997 |
| K964833 | RMI DUAL FLUID IRRIGATING SYRINGE | February 19, 1997 |
| K961927 | RMI HEMOCONCENTRACTOR TUBING SET | August 13, 1996 |
| K960098 | RMI INTERNAL MAMMARY ARTERY CANNULA | March 26, 1996 |
| K951344 | RMI HEMOCONCENTRATOR | August 15, 1995 |
| K922083 | RMI SURGICCAL SITE VISUALIZATION WAND | January 29, 1993 |
| K920936 | RMI EXTERNAL CORONARY ARTERY OCCLUDER | December 18, 1992 |
| K915869 | RMI NORMOCLUDER CORONARY ARTERY OCCLUDER | December 8, 1992 |
| K920676 | RMI SOFCLAMP | April 15, 1992 |
| K910221 | RMI VASCULAR TOURNIQUET KIT | May 16, 1991 |
| K901231 | RMI CARDIOPLEGIA DELIVERY KITS | June 8, 1990 |
| K897137 | RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORING | March 27, 1990 |
| K896777 | RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE | February 27, 1990 |
| K896778 | RMI VASOPLEGIA CANNULA WITH & WITHOUT CHECK VALVE | February 27, 1990 |
| K896636 | RMI ANTEPLEGIA CANNULA | February 15, 1990 |
| K892377 | RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SET | December 7, 1989 |
| K892368 | RMI CARDIOPLEGIA DELIVERY SETS | December 7, 1989 |
| K891576 | FEM-FLEX FEMORAL ACCESS CANNULATION SET | October 12, 1989 |
| K894243 | RMI ARTERIAL PERFUSION CANNULA | September 19, 1989 |
| K880103 | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. | March 22, 1988 |