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MODEL 3587A RESUME EPIDURAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K884948
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1989
Days to Decision
53 days

MODEL 3587A RESUME EPIDURAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K884948
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1989
Days to Decision
53 days