FDA 510(k), K033275, LIFEPAK 12, 20, 500, CR PLUS
FDA 510(k), K033275, LIFEPAK 12, 20, 500, CR PLUS
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$149.00 USD
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$149.00 USD
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510(K) Number: K033275
Device Name: LIFEPAK 12, 20, 500, CR PLUS
Manufacturer:
Device Classification Name: Automated External Defibrillators (Non-Wearable)
Regulation Number: 870.5310
Classification Product Code: MKJ
Date Received: 10/10/2003
Decision Date: 11/06/2003
Regulation Medical Specialty: Cardiovascular
Device Name: LIFEPAK 12, 20, 500, CR PLUS
Manufacturer:
Device Classification Name: Automated External Defibrillators (Non-Wearable)
Regulation Number: 870.5310
Classification Product Code: MKJ
Date Received: 10/10/2003
Decision Date: 11/06/2003
Regulation Medical Specialty: Cardiovascular