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GUIDEWIRE INTRODUCER SAFETY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K011085
510(k) Type
Traditional
Applicant
MEDAMICUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2001
Days to Decision
90 days
Submission Type
Summary

GUIDEWIRE INTRODUCER SAFETY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K011085
510(k) Type
Traditional
Applicant
MEDAMICUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2001
Days to Decision
90 days
Submission Type
Summary