Class Class II

Galaxy System (K223144)

K223144 2023-03-01 Traditional
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Description

Galaxy System by Noah Medical Corp. — FDA 510(k) cleared ear, nose, throat device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223144
Clearance Date2023-03-01
Clearance TypeTraditional
Product CodeEOQ
Regulation Number874.4680

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