Last synced on 9 December 2022 at 11:04 pm

EndoFLIP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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