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Regulation & law · 23/12/1996

FDA Approves VISX Excimer Laser System for Phototherapeutic Keratectomy

The US Food and Drug Administration (FDA) has granted premarket approval for VISX, Inc.'s Excimer Laser System (Models B and C) for use in phototherapeutic keratectomy procedures, following a recommendation from the Ophthalmic Devices Panel.

Original source language: Federal Register — All DocumentsOpen original release →

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