Class Class II

Spencer Probe Depth Electrodes (K223269)

K223269 2023-05-18 Traditional
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Description

Spencer Probe Depth Electrodes by Ad-Tech Medical Instrument Corporation — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223269
Clearance Date2023-05-18
Clearance TypeTraditional
Product CodeGZL
Regulation Number882.1330

Categories

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