Research Medical, Inc.
Mchenry, IL, US
Research Medical, Inc. appears in FDA device records in Mchenry, IL. FDA records list 35 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 35
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 35 510(k) clearances for Research Medical, Inc. between 1984 and 1997. The busiest year on record is 1986, with 5. The most recent is 1997, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 2 |
| 1985 | 4 |
| 1986 | 5 |
| 1987 | 4 |
| 1988 | 1 |
| 1989 | 4 |
| 1990 | 5 |
| 1991 | 1 |
| 1992 | 3 |
| 1993 | 1 |
| 1995 | 1 |
| 1996 | 2 |
| 1997 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K970739 | RMI HEMOCONCENTRATOR PREFERENCE PACK | KDI | Substantially Equivalent | |
| K964833 | RMI DUAL FLUID IRRIGATING SYRINGE | KYZ | Substantially Equivalent | |
| K961927 | RMI HEMOCONCENTRACTOR TUBING SET | DWF | Substantially Equivalent | |
| K960098 | RMI INTERNAL MAMMARY ARTERY CANNULA | DQR | Substantially Equivalent | |
| K951344 | RMI HEMOCONCENTRATOR | KDI | Substantially Equivalent | |
| K922083 | RMI SURGICCAL SITE VISUALIZATION WAND | FQH | Substantially Equivalent | |
| K920936 | RMI EXTERNAL CORONARY ARTERY OCCLUDER | DXC | Substantially Equivalent | |
| K915869 | RMI NORMOCLUDER CORONARY ARTERY OCCLUDER | MJN | Substantially Equivalent | |
| K920676 | RMI SOFCLAMP | DSS | Substantially Equivalent | |
| K910221 | RMI VASCULAR TOURNIQUET KIT | DXC | Substantially Equivalent | |
| K901231 | RMI CARDIOPLEGIA DELIVERY KITS | DWF | Substantially Equivalent | |
| K897137 | RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORING | DTL | Substantially Equivalent | |
| K896778 | RMI VASOPLEGIA CANNULA WITH & WITHOUT CHECK VALVE | DWF | Substantially Equivalent | |
| K896777 | RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE | DWF | Substantially Equivalent | |
| K896636 | RMI ANTEPLEGIA CANNULA | DWF | Substantially Equivalent | |
| K892377 | RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SET | DTL | Substantially Equivalent | |
| K892368 | RMI CARDIOPLEGIA DELIVERY SETS | DTL | Substantially Equivalent | |
| K891576 | FEM-FLEX FEMORAL ACCESS CANNULATION SET | DWF | Substantially Equivalent | |
| K894243 | RMI ARTERIAL PERFUSION CANNULA | DQR | Substantially Equivalent | |
| K880103 | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. | DWF | Substantially Equivalent | |
| K870421 | TDMAC-HEPARIN COATED RMI | DWF | Substantially Equivalent | |
| K870507 | GRUNWALD BI-CAVAL & JONES BI-CAVAL CANNULA | DWF | Substantially Equivalent | |
| K870109 | RMI VENOUS DRAINAGE CANNULA | DWF | Substantially Equivalent | |
| K863740 | RMI FEMORAL VENOUS DRAINAGE CANNULA | DWF | Substantially Equivalent | |
| K862634 | TDMAC-HEPARIN COATED RMI CAROTID BY-PASS SHUNT | DWF | Substantially Equivalent | |
| K861790 | RMI BALLOON-OCCLUSIVE CAROTID BY-PASS SHUNT | DWF | Substantially Equivalent | |
| K861322 | RMI POROUS VENT PLUG | DWF | Substantially Equivalent | |
| K860988 | RMI CAROTID BY-PASS SHUNT | DWF | Substantially Equivalent | |
| K854812 | NELSON-JUNG PLEURAL CATH | GBW | Substantially Equivalent | |
| K852197 | LAP-CATH | DQO | Substantially Equivalent | |
| K852456 | FAP-CATH | DQO | Substantially Equivalent | |
| K850785 | FASTUBE NERVE REGENERATION DEVICE | JXI | Substantially Equivalent | |
| K843423 | PHYSIO GAS ANALYZER | LLL | Substantially Equivalent | |
| K841425 | JINOTTI OXYGEN/SUCTION CATHETER | BSY | Substantially Equivalent | |
| K841727 | UROLOGICAL CATHETER & ACCESSORIES | KOD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- DQRCannula, Catheter
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- MJNCatheter, Intravascular Occluding, Temporary
- DQOCatheter, Intravascular, Diagnostic
- GBWCatheter, Peritoneal
- KODCatheter, Urological
- BSYCatheters, Suction, Tracheobronchial
- DXCClamp, Vascular
- DSSClip, Vascular
- JXICuff, Nerve
- KDIDialyzer, High Permeability With Or Without Sealed Dialysate System
- LLLExtractable Antinuclear Antibody, Antigen And Control
- FQHLavage, Jet
- KYZSyringe, Irrigating (Non Dental)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
