Last synced on 6 June 2025 at 11:06 pm

LIFEPAK 20 DEFIBRILLATOR/ MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063119
510(k) Type
Special
Applicant
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
71 days
Submission Type
Summary

LIFEPAK 20 DEFIBRILLATOR/ MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063119
510(k) Type
Special
Applicant
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
71 days
Submission Type
Summary