Class Class II

ENT EM (K223734)

K223734 2023-04-27 Traditional
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Description

ENT EM by Brainlab AG — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223734
Clearance Date2023-04-27
Clearance TypeTraditional
Product CodePGW
Regulation Number882.4560

Categories

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