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ROSE K POST GRAFT LENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013646
510(k) Type
Traditional
Applicant
ROSE K INTERNATIONAL LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
5/30/2002
Days to Decision
206 days
Submission Type
Statement

ROSE K POST GRAFT LENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013646
510(k) Type
Traditional
Applicant
ROSE K INTERNATIONAL LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
5/30/2002
Days to Decision
206 days
Submission Type
Statement