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MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012274
510(k) Type
Traditional
Applicant
Medtronic Physio-Control Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2002
Days to Decision
201 days
Submission Type
Summary

MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012274
510(k) Type
Traditional
Applicant
Medtronic Physio-Control Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2002
Days to Decision
201 days
Submission Type
Summary