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PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K946080
510(k) Type
Traditional
Applicant
PORTABLE POWER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1995
Days to Decision
232 days
Submission Type
Statement

PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K946080
510(k) Type
Traditional
Applicant
PORTABLE POWER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1995
Days to Decision
232 days
Submission Type
Statement