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ESTECH EASYFLOW CANNULA WITH GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091542
510(k) Type
Traditional
Applicant
ENDOSCOPIC TECHNOLOGIES, INC. D/B/A ESTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2009
Days to Decision
147 days
Submission Type
Summary

ESTECH EASYFLOW CANNULA WITH GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091542
510(k) Type
Traditional
Applicant
ENDOSCOPIC TECHNOLOGIES, INC. D/B/A ESTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2009
Days to Decision
147 days
Submission Type
Summary