Class Class II

Talee, Talee PostOp (K241957)

K241957 2024-08-30 Traditional
Home/ Devices/ Talee, Talee PostOp (K241957)

Description

Talee, Talee PostOp by Invent Medical USA, LLC — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241957
Clearance Date2024-08-30
Clearance TypeTraditional
Product CodeMVA
Regulation Number882.5970

Categories

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