Last synced on 14 November 2025 at 11:06 pm

VISITEC CANALICULAR STENT

Page Type
Cleared 510(K)
510(k) Number
K915809
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1992
Days to Decision
62 days
Submission Type
Summary

VISITEC CANALICULAR STENT

Page Type
Cleared 510(K)
510(k) Number
K915809
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1992
Days to Decision
62 days
Submission Type
Summary