FDA 510(k), K935674, LIFEPAK 9 DEFIBRILLATOR/MONITOR
FDA 510(k), K935674, LIFEPAK 9 DEFIBRILLATOR/MONITOR
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$149.00 USD
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510(K) Number: K935674
Device Name: LIFEPAK 9 DEFIBRILLATOR/MONITOR
Manufacturer:
Device Classification Name: Dc-Defibrillator, Low-Energy, (Including Paddles)
Regulation Number: 870.5300
Classification Product Code: LDD
Date Received: 12/08/1993
Decision Date: 12/16/1993
Regulation Medical Specialty: Cardiovascular
Device Name: LIFEPAK 9 DEFIBRILLATOR/MONITOR
Manufacturer:
Device Classification Name: Dc-Defibrillator, Low-Energy, (Including Paddles)
Regulation Number: 870.5300
Classification Product Code: LDD
Date Received: 12/08/1993
Decision Date: 12/16/1993
Regulation Medical Specialty: Cardiovascular