MICROSTAAR INJECTOR MODELS MSI-TD & MSI-PD (MODIFICATION)

MICROSTAAR INJECTOR MODELS MSI-TD & MSI-PD (MODIFICATION) is an FDA 510(k)-cleared medical device (K954600) manufactured by Staar Surgical Co.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 20, 1995. Regulation: 8.