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LIFEPAK 9 DEFIBRILLATOR/MONITOR

Page Type
Cleared 510(K)
510(k) Number
K935674
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1993
Days to Decision
8 days
Submission Type
Summary

LIFEPAK 9 DEFIBRILLATOR/MONITOR

Page Type
Cleared 510(K)
510(k) Number
K935674
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1993
Days to Decision
8 days
Submission Type
Summary