Kontron Instruments, Inc.
57 devices
Public registrations
1 cert. types · 57 public registrations
- FDA 510(k)
- Main field
- Other
Aggregated from registration data published by national regulators. It is not a count of currently valid certifications and may include expired or withdrawn records. Some registrations do not state a manufacturing country.
Products
- MODIFICATIONS TO INTRA-AORTIC BALLOONSOtherFDA 510(k)
- MODIFICATION OF INTRA-AORTIC BALLOON CATHETERSOtherFDA 510(k)
- INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATIONOtherFDA 510(k)
- KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT IIOtherFDA 510(k)
- 9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)OtherFDA 510(k)
- KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEMOtherFDA 510(k)
- 9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOONOtherFDA 510(k)
- SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283Patient MonitoringFDA 510(k)
- MINIMON 7133B PATIENT MONITORCardiologyFDA 510(k)
- KONTRON KOLORMON 7250 PATIENT MONITORCardiologyFDA 510(k)
- MINIMON 7137B PATIENT MONITORPatient MonitoringFDA 510(k)
- 10 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOONOtherFDA 510(k)
- 8 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOONOtherFDA 510(k)
- 9 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOONOtherFDA 510(k)
- KONTRON INTRA-AORTIC BALLOON PUMP MODEL K9000OtherFDA 510(k)
- SUPERMON ARRHYTHMIA MODULE 7270Patient MonitoringFDA 510(k)
- 10.5 FRENCH PERCUTANEOUS DOUBLE LUMEN INTRA-AORTICOtherFDA 510(k)
- 9.5 FRENCH PERCUTANEOUS DOUBLE LUMEN BALLOONOtherFDA 510(k)
- KONTRON PULSE OXIMETER 7840Patient MonitoringFDA 510(k)
- MINIMON 7134B PATIENT MONITOROtherFDA 510(k)
- KONTRON PULSE OXIMETER 7840Patient MonitoringFDA 510(k)
- MINIMON 7131B PATIENT MONITORCardiologyFDA 510(k)
- MINIMON 7132B PATIENT MONITORCardiologyFDA 510(k)
- SIGMA 1 WOBBLER BIOPSY KITOtherFDA 510(k)
- KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281OtherFDA 510(k)
- INTRA-AORTIC BALLOON PUMP MODEL KAATOtherFDA 510(k)
- KONTRON INTRA-AORTIC BALLOON PUMP MODEL K2000OtherFDA 510(k)
- KONTRON SIGMA 1 DIGITAL ECHOCARDIOGRAPH SYSTEMOtherFDA 510(k)
- KONTRON SIGMA 1 DIGITAL ECHOCARDIOGRAPH SYSTEMOtherFDA 510(k)
- KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEMPatient MonitoringFDA 510(k)
- KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265OtherFDA 510(k)
- SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282Patient MonitoringFDA 510(k)
- KONTRON SIGMA 1SC DIGITAL ECHOCARDIOGRAPHY SYSTEMDiagnostic ImagingFDA 510(k)
- KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263OtherFDA 510(k)
- KONTRON VITALMON 5010 PATIENT MONITOROtherFDA 510(k)
- NOVEMPERC DOUBLE LUMEN INTRA-AORTIC BALLOONOtherFDA 510(k)
- KONTRON INTRA-AORTIC BALLOON PUMP MODEL KAATOtherFDA 510(k)
- KONTRON CUTANEOUS PO2 MONITOR 820OtherFDA 510(k)
- INTRA-AORTIC BALLOON PUMP MODEL K2000OtherFDA 510(k)
- KONTRON DEFIBRILLATOR 7501OtherFDA 510(k)
- KONTRON FAX FETAL MONITOROtherFDA 510(k)
- KONTRON SIGMA ISC ECHOCARDIOGRAPH SYSTEMOtherFDA 510(k)
- KONTRON SUPERMON 7210 PATIENT MONITOROtherFDA 510(k)
- KONTRON MINIMON 7134 PATIENT MONITOROtherFDA 510(k)
- KONTRON MINIMON 7131 PATIENT MONITOROtherFDA 510(k)
- KONTRON MINIMON 7132 PATIENT MONITOROtherFDA 510(k)
- TRANSDUCER FOR KONTROL 5MHZ SIGMA 20OtherFDA 510(k)
- SIGMA 20 ELECTRONIC SECTOR SCANNERDiagnostic ImagingFDA 510(k)
- TEMPERATURE MODULE 242-100OtherFDA 510(k)
- MULTI-PRONG FETAL SCALP ELECTRODEOtherFDA 510(k)
- ABT 4000 VENTILATOROtherFDA 510(k)
- KONTRON LITWAK-KOFFSKY OBTURATED CANNUOtherFDA 510(k)
- ADAPTATION OF KANTRON 40 CC. PDLIABOtherFDA 510(k)
- ZIKON 100 DIGITAL X-RAY SYSTEMOtherFDA 510(k)
- FETASONDE 5, #30, CENTRAL NURSING STATOtherFDA 510(k)
- KONTRON PMS 7000OtherFDA 510(k)
- MS-50 ULTRASONIC IMAGERDiagnostic ImagingFDA 510(k)