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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
510(k) clearance decisions for Research Medical, Inc., by decision year
YearClearances
19842
19854
19865
19874
19881
19894
19905
19911
19923
19931
19951
19962
19972
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K970739RMI HEMOCONCENTRATOR PREFERENCE PACKKDISubstantially Equivalent
K964833RMI DUAL FLUID IRRIGATING SYRINGEKYZSubstantially Equivalent
K961927RMI HEMOCONCENTRACTOR TUBING SETDWFSubstantially Equivalent
K960098RMI INTERNAL MAMMARY ARTERY CANNULADQRSubstantially Equivalent
K951344RMI HEMOCONCENTRATORKDISubstantially Equivalent
K922083RMI SURGICCAL SITE VISUALIZATION WANDFQHSubstantially Equivalent
K920936RMI EXTERNAL CORONARY ARTERY OCCLUDERDXCSubstantially Equivalent
K915869RMI NORMOCLUDER CORONARY ARTERY OCCLUDERMJNSubstantially Equivalent
K920676RMI SOFCLAMPDSSSubstantially Equivalent
K910221RMI VASCULAR TOURNIQUET KITDXCSubstantially Equivalent
K901231RMI CARDIOPLEGIA DELIVERY KITSDWFSubstantially Equivalent
K897137RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORINGDTLSubstantially Equivalent
K896778RMI VASOPLEGIA CANNULA WITH & WITHOUT CHECK VALVEDWFSubstantially Equivalent
K896777RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINEDWFSubstantially Equivalent
K896636RMI ANTEPLEGIA CANNULADWFSubstantially Equivalent
K892377RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SETDTLSubstantially Equivalent
K892368RMI CARDIOPLEGIA DELIVERY SETSDTLSubstantially Equivalent
K891576FEM-FLEX FEMORAL ACCESS CANNULATION SETDWFSubstantially Equivalent
K894243RMI ARTERIAL PERFUSION CANNULADQRSubstantially Equivalent
K880103CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.DWFSubstantially Equivalent
K870421TDMAC-HEPARIN COATED RMIDWFSubstantially Equivalent
K870507GRUNWALD BI-CAVAL & JONES BI-CAVAL CANNULADWFSubstantially Equivalent
K870109RMI VENOUS DRAINAGE CANNULADWFSubstantially Equivalent
K863740RMI FEMORAL VENOUS DRAINAGE CANNULADWFSubstantially Equivalent
K862634TDMAC-HEPARIN COATED RMI CAROTID BY-PASS SHUNTDWFSubstantially Equivalent
K861790RMI BALLOON-OCCLUSIVE CAROTID BY-PASS SHUNTDWFSubstantially Equivalent
K861322RMI POROUS VENT PLUGDWFSubstantially Equivalent
K860988RMI CAROTID BY-PASS SHUNTDWFSubstantially Equivalent
K854812NELSON-JUNG PLEURAL CATHGBWSubstantially Equivalent
K852197LAP-CATHDQOSubstantially Equivalent
K852456FAP-CATHDQOSubstantially Equivalent
K850785FASTUBE NERVE REGENERATION DEVICEJXISubstantially Equivalent
K843423PHYSIO GAS ANALYZERLLLSubstantially Equivalent
K841425JINOTTI OXYGEN/SUCTION CATHETERBSYSubstantially Equivalent
K841727UROLOGICAL CATHETER & ACCESSORIESKODSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain