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HEADWAY DUO MICROCATHETER

Page Type
Cleared 510(K)
510(k) Number
K120917
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2012
Days to Decision
128 days
Submission Type
Summary

HEADWAY DUO MICROCATHETER

Page Type
Cleared 510(K)
510(k) Number
K120917
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2012
Days to Decision
128 days
Submission Type
Summary