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MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012428
510(k) Type
Special
Applicant
Medtronic Physio-Control Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2001
Days to Decision
59 days
Submission Type
Summary

MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012428
510(k) Type
Special
Applicant
Medtronic Physio-Control Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2001
Days to Decision
59 days
Submission Type
Summary