LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES


definition

Device Classification Name

automated external defibrillators (non-wearable)

510(k) Number K002445
Device Name LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES
Original Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
11811 willows rd., n.e.
redmond, 
WA 
98073

Original Contact bob zito
Regulation Number 870.5310
Classification Product Code
MKJ  
Subsequent Product Code
DSK  
Date Received 08/09/2000
Decision Date 01/31/2001
Decision

(ST)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls