FDA 510(k) Applications Submitted by OPTONOL, LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030350 | 02/03/2003 | EXPRESS MINI GLAUCOMA SHUNT | OPTONOL, LTD |
| K012852 | 08/24/2001 | EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONS | OPTONOL, LTD |
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