Class Class I

EyeGility™ Inserter for Preloaded enVista IOLs (K242389)

K242389 2024-10-10 Traditional
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Description

EyeGility™ Inserter for Preloaded enVista IOLs by Bausch & Lomb Incorporated — FDA 510(k) cleared ophthalmic device.

Regulatory Information

Device ClassClass Class I
510(k) NumberK242389
Clearance Date2024-10-10
Clearance TypeTraditional
Product CodeMSS
Regulation Number886.4300

Categories

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