Class Class U

Retraxil (K243910)

K243910 2025-09-24 Traditional
Home/ Devices/ Retraxil (K243910)

Description

Retraxil by Kulzer, LLC, an FDA 510(k) cleared unknown device.

Regulatory Information

Device ClassClass Class U
510(k) NumberK243910
Clearance Date2025-09-24
Clearance TypeTraditional
Product CodeMVL

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