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EXPRESS MINI GLAUCOMA SHUNT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030350
510(k) Type
Abbreviated
Applicant
OPTONOL, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2003
Days to Decision
38 days
Submission Type
Summary

EXPRESS MINI GLAUCOMA SHUNT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030350
510(k) Type
Abbreviated
Applicant
OPTONOL, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2003
Days to Decision
38 days
Submission Type
Summary