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CHAPERON GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K082385
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2008
Days to Decision
114 days
Submission Type
Summary

CHAPERON GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K082385
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2008
Days to Decision
114 days
Submission Type
Summary