FDA 510(k) Applications Submitted by NO 7 CONTACT LENS LABORATORY LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032256 | 07/22/2003 | QUASAR-QUASAR PLUS-QUASAR TORIC (HYBUFOCON A, HEXAFOCON A, PAFLUFOCON B) RIGID GAS PERMEABLE (RGP) DAILY WEAR CONTACT LE | NO 7 CONTACT LENS LABORATORY LTD. |
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