Class Class II

INSULCLOCK® v2.0 PRO (K241803)

K241803 2024-08-22 Traditional
Home/ Devices/ INSULCLOCK® v2.0 PRO (K241803)

Description

INSULCLOCK® v2.0 PRO by Insulcloud S.L. — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241803
Clearance Date2024-08-22
Clearance TypeTraditional
Product CodeQOG
Regulation Number880.5860

Categories

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