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LIFEPAK 15 MONITOR/DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103567
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2011
Days to Decision
106 days
Submission Type
Summary

LIFEPAK 15 MONITOR/DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103567
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2011
Days to Decision
106 days
Submission Type
Summary