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EndoFLIP

Page Type
Cleared 510(K)
510(k) Number
K160725
510(k) Type
Traditional
Applicant
CROSPON LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/1/2016
Days to Decision
46 days
Submission Type
Summary

EndoFLIP

Page Type
Cleared 510(K)
510(k) Number
K160725
510(k) Type
Traditional
Applicant
CROSPON LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/1/2016
Days to Decision
46 days
Submission Type
Summary