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FDA 510(k), K103783, EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC
FDA 510(k), K103783, EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC
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510(K) Number: K103783
Device Name: EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC
Manufacturer: FIAB S.P.A.
Device Classification Name: Dc-Defibrillator, Low-Energy, (Including Paddles)
Regulation Number: 870.5300
Classification Product Code: LDD
Date Received: 12/27/2010
Decision Date: 06/16/2011
Regulation Medical Specialty: Cardiovascular
Device Name: EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC
Manufacturer: FIAB S.P.A.
Device Classification Name: Dc-Defibrillator, Low-Energy, (Including Paddles)
Regulation Number: 870.5300
Classification Product Code: LDD
Date Received: 12/27/2010
Decision Date: 06/16/2011
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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