4,665 results · 78ms · Sources: EU EUDAMED, US FDA

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval
FDA Class 3 ·Multifunctional Ablation Generator (MAG)

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval
FDA Class 3 ·Synergy Ablation System

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval
FDA Class 3 ·ATRICURE SYNERGY ABLATION SYSTEM

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval
FDA Class 3 ·AtriCure Isolator Clamp, AtriCure Long Clamp, AtriCure Synergy Clamp

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA classification
FDA Class 3 ·Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

OLYMPUS ULTRASONIC SURGICAL SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

ULTRACISION HARMONIC SCALPEL SHARP CURVED BLADE/FAST BLADE, MODEL HF105

FDA 510(k)
FDA Unclassified ·Unknown

ULTRACISION HARMONIC SCALPEL HAND PIECE

FDA 510(k)
FDA Unclassified ·Unknown

ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-5

FDA 510(k)
FDA Unclassified ·Unknown

CUSA Clarity Ultrasonic Surgical Aspirator System

FDA 510(k)
FDA Unclassified ·Unknown

neXus Ultrasonic Surgical Aspirator System

FDA 510(k)
FDA Unclassified ·Unknown

R PAK

FDA 510(k)
FDA Unclassified ·Unknown

CUSA Clarity Ultrasonic Surgical Aspirator System

FDA 510(k)
FDA Unclassified ·Unknown

SONOCA 180/195 WOUND CARE SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

OLYMPUS ULTRASONIC SURGICAL SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA

FDA 510(k)
FDA Unclassified ·Unknown

ULTRA-SAFE ULTRASONIC ASPIRATOR SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

CUSA EXCEL ULTRASONIC SURGICAL ASPIRATOR SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RF

FDA 510(k)
FDA Unclassified ·Unknown

neXus Ultrasonic Surgical Aspirator System

FDA 510(k)
FDA Unclassified ·Unknown