1,496 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·CELSIUS II DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER THERMOCOUPLE OR THERMISTOR
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·CELSIUS and EZ STEER
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·NAVISTAR ELECTROPHYSIOLOGY CATHETER
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·NAVI-STAR DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·Navistar RMT Electrophysiology Catheter
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·NAVISTAR Electrophysiology Catheter, EZ Steer NAV Bi-Directional Electrophysiology Catheter, NAVISTAR RMT Electrophysiol
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·CELSIUS DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·STOCKERT 70 RF GENERATOR WITH SOFTWARE VERSION 1.033
TriVerity
FDA 510(k)
FDA Class 2
·Microbiology
SeptiCyte RAPID
FDA 510(k)
FDA Class 2
·Microbiology
SeptiCyte LAB
FDA 510(k)
FDA Class 2
·Microbiology
SeptiCyte RAPID
FDA 510(k)
FDA Class 2
·Microbiology
FIBRINOSTIKA(R) FGDP MICROELISA SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
SPECTRASCAN
FDA 510(k)
FDA Class 2
·Hematology
PAXGENE BLOOD RNA SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
MODIFICATION TO PAXGENE BLOOD RNA SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
Sterilizer, Dry Heat
FDA classification
FDA Class 2
·Sterilizer, Dry Heat
Full Field Digital, System, X-Ray, Mammographic
FDA Pre-Market Approval
FDA Class 2
·GEMS SENOGRAPHE 2000D FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM
Intense Pulsed Light Device For Managing Dry Eye
FDA classification
FDA Class 2
·Intense Pulsed Light Device For Managing Dry Eye
Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control
FDA classification
FDA Class 2
·Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control