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PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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