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MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K012428
510(k) Type
Special
Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2001
Days to Decision
59 days
Submission Type
Summary

MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K012428
510(k) Type
Special
Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2001
Days to Decision
59 days
Submission Type
Summary