FDA 510(k), K000795, RIGID GAS PERMEABLE CONTACT LENS
FDA 510(k), K000795, RIGID GAS PERMEABLE CONTACT LENS
Device Name: RIGID GAS PERMEABLE CONTACT LENS
Manufacturer:
Device Classification Name: Lens, Contact (Other Material) - Daily
Regulation Number: 886.5916
Classification Product Code: HQD
Date Received: 03/13/2000
Decision Date: 05/26/2000
Regulation Medical Specialty: Ophthalmic
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