Class Class II

InSee (K241152)

K241152 2025-08-21 Traditional
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Description

InSee by Tidal Medical Technologies, LLC, an FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241152
Clearance Date2025-08-21
Clearance TypeTraditional
Product CodeBWF
Regulation Number868.5690

Categories

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