10,000 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LiveWire TC Steerable Electrophysiology Catheter
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·SAFIRE ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LIVEWIRE TC ABLATION CATHETER, SAFIRE ABLATION CATHETER
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LIVEWIRE TC CARDIAC ABLATION SYSTEM-ADDITION OF LIVEWIRE TC STEERABLE ELECTROPHYSIOLOGY
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LIVEWIRE TC STEERABLE ELECTROPHYSIOLOGY CATHETER
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LIVEWIRE TC STEERABLE ELECTROPHYSIOLOGY CATHETER, SAFIRE BI-DIRECTIONAL ABLATION CATHETER
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LIVEWIRE TC CARDIAC ABLATION SYSTEM
LINK METAL-BACKED ACETABULAR CUPS
FDA 510(k)
FDA Class 3
·Orthopedic
LIDGRER-LUND ACETABULAR SOCKETS
FDA 510(k)
FDA Class 3
·Orthopedic
Total, Prostate Specific Antigen (Noncomplexed & Complexed) For Detection Of Prostate Cancer
FDA Pre-Market Approval
FDA Class 3
·ABBOTT IMX TOTAL PSA, ABBOTT AXSYM TOTAL PSA AND ABBOTT ARCHITECT TOTAL PSA
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilatation Balloon System with Integrated Embolic Protection
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Neuroguard IEP 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection
Kit, Test, In Vitro Periodontal
FDA Pre-Market Approval
FDA Class 3
·PERIOCHECK TM ENZYME ACTIVITY TEST KIT
Kit, Test, In Vitro Periodontal
FDA Pre-Market Approval
FDA Class 3
·PERIOCHECK TM ENZYME ACTIVITY TEST KIT
THERAPEUTIC EXCHANGE SYSTEM
FDA 510(k)
FDA Class 3
·Unknown
Fluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)
FDA Pre-Market Approval
FDA Class 3
·Vysis CLL FISH Probe Kit
Fluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)
FDA Pre-Market Approval
FDA Class 3
·Vysis CLL FISH Probe Kit
Fluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)
FDA Pre-Market Approval
FDA Class 3
·Vysis CLL FISH Probe Kit
Fluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)
FDA Pre-Market Approval
FDA Class 3
·Vysis CLL FISH Probe Kit