Medical Device Catalogue

305 devices foundsorted by relevance

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Ensite System

Endocardial Solutions, Inc.,United States(FDA 510(k) applicant) Class II

Active 510(k) 510(k) II
EnSite™ X EP System

Abbott Medical,Ireland Class II

Active 510(k) 510(k) II
7 variants
- EnSite™ X EP System K260212
- See all variants of this device
EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2

Abbott,FDA registration: Germany Class II

Active 510(k) 510(k) II
2 variants
- See all variants of this device
Ensite 3000 System, Model EE3000

Endocardial Solutions, Inc.,United States(FDA 510(k) applicant) Class II

Active 510(k) 510(k) II
EnSite Velocity Surface Electrode Kit

St Jude Medical,FDA registration: United States Class II

Active 510(k) 510(k) II
Ensite Velocity System, Model EE3000

St Jude Medical,FDA registration: United States Class II

Active 510(k) 510(k) II
Ensite System, Model EE3000

Endocardial Solutions, Inc.,United States(FDA 510(k) applicant) Class II

Active 510(k) 510(k) II
Modification To Ensite 3000 System, Model EE3000

Endocardial Solutions, Inc.,United States(FDA 510(k) applicant) Class II

Active 510(k) 510(k) II
2 variants
- Modification To Ensite 3000 System, Model EE3000 K030129
EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software Upgrade; EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software License

Abbott Medical,Ireland Class II

Active 510(k) 510(k) II
EnSite Precision Cardiac Mapping System v2.6, EnSite Precision Software Installation v2.6, EnSite LiveView Dynamic Display Software License

Abbott Medical,Ireland Class II

Active 510(k) 510(k) II
Modification To Ensite System, Model EE3000

St. Jude Medical, Inc.-Endocardial Solutions,FDA registration: United States Class II

Active 510(k) 510(k) II
Ensite Velocity System

St Jude Medical,FDA registration: United States Class II

Active 510(k) 510(k) II
5 variants
- Ensite Velocity System K110549
- Ensite Velocity System K130594
- See all variants of this device
Ensite Velocity System V1.3

St Jude Medical,FDA registration: United States Class II

Active 510(k) 510(k) II
Modification To: Ensite System, Model, EE3000

St Jude Medical,FDA registration: United States Class II

Active 510(k) 510(k) II
SiteSeal Femoral Compression Device

Ensite Vacular, LLC,FDA registration: United States Class II

Active 510(k) 510(k) II
EnSite Velocity Cardiac Mapping System v5.2

St Jude Medical,FDA registration: United States Class II

Active 510(k) 510(k) II

Showing 281-300 of 305

Results for “EnSite™”

Category (EMDN)

Ensite System

EnSite™ X EP System

EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2

Ensite 3000 System, Model EE3000

EnSite Velocity Surface Electrode Kit

Ensite Velocity System, Model EE3000

Ensite System, Model EE3000

Modification To Ensite 3000 System, Model EE3000

EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software Upgrade; EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software License

EnSite Precision Cardiac Mapping System v2.6, EnSite Precision Software Installation v2.6, EnSite LiveView Dynamic Display Software License

Modification To Ensite System, Model EE3000

Ensite Velocity System

Ensite Velocity System V1.3

Modification To: Ensite System, Model, EE3000

SiteSeal Femoral Compression Device

EnSite Velocity Cardiac Mapping System v5.2