365 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Powerheart G5 AED
FDA 510(k)
FDA Class 3
·Cardiovascular
POWERHEART AED G3A
FDA 510(k)
FDA Class 3
·Cardiovascular
POWERHEART G5 AED
FDA 510(k)
FDA Class 3
·Cardiovascular
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart® G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart® G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart® G3, G3 Plus and G5 AEDs
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·GORE® CARDIOFORM Septal Occluder, GORE® CARDIOFORM ASD Occluder
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RADIESSE,RADIESSE (+) LIDOCAINE DERMAL FILLER
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RADIESSE INJECTABLE IMPLANT
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula® System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula® System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula® System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula® System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula® System
Tympanostomy Tube Delivery Product With Drug
FDA Pre-Market Approval
FDA Class 3
·Tula System