Last synced on 14 November 2025 at 11:06 pm

MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626

Page Type
Cleared 510(K)
510(k) Number
K022238
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2002
Days to Decision
90 days
Submission Type
Summary

MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626

Page Type
Cleared 510(K)
510(k) Number
K022238
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2002
Days to Decision
90 days
Submission Type
Summary