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DURETTE OCULAR IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123764
510(k) Type
Traditional
Applicant
OCULO-PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
1/31/2013
Days to Decision
55 days
Submission Type
Summary

DURETTE OCULAR IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123764
510(k) Type
Traditional
Applicant
OCULO-PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
1/31/2013
Days to Decision
55 days
Submission Type
Summary