Last synced on 2 December 2022 at 11:04 pm

EndoFLIP System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183072
510(k) Type
Traditional
Applicant
Crospon Ltd
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
2/15/2019
Days to Decision
102 days
Submission Type
Summary

EndoFLIP System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183072
510(k) Type
Traditional
Applicant
Crospon Ltd
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
2/15/2019
Days to Decision
102 days
Submission Type
Summary