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ENDOFLIP CATHETER

Page Type
Cleared 510(K)
510(k) Number
K130906
510(k) Type
Traditional
Applicant
CROSPON, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2013
Days to Decision
107 days
Submission Type
Summary

ENDOFLIP CATHETER

Page Type
Cleared 510(K)
510(k) Number
K130906
510(k) Type
Traditional
Applicant
CROSPON, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2013
Days to Decision
107 days
Submission Type
Summary