Class Class II

EsoCheck Cell Collection Device (K230339)

K230339 2023-02-24 Special
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Description

EsoCheck Cell Collection Device by Lucid Diagnostics, Inc. — FDA 510(k) cleared ear, nose, throat device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230339
Clearance Date2023-02-24
Clearance TypeSpecial
Product CodeEOX
Regulation Number874.4710

Categories

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