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LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES

Page Type
Cleared 510(K)
510(k) Number
K002445
510(k) Type
Traditional
Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
1/31/2001
Days to Decision
175 days

LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES

Page Type
Cleared 510(K)
510(k) Number
K002445
510(k) Type
Traditional
Applicant
MEDTRONIC PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
1/31/2001
Days to Decision
175 days