Class Class II

MiniMed Go App (K253512)

K253512 2026-01-08 Traditional
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Description

MiniMed Go App by Medtronic Minimed, an FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253512
Clearance Date2026-01-08
Clearance TypeTraditional
Product CodeNDC
Regulation Number868.1890

Categories

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