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LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K010918
510(k) Type
Traditional
Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/23/2001
Days to Decision
149 days

LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K010918
510(k) Type
Traditional
Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/23/2001
Days to Decision
149 days