Class Class U

TRAUMAGEL® (K240713)

K240713 2024-08-14 Traditional
Home/ Devices/ TRAUMAGEL® (K240713)

Description

TRAUMAGEL® by Cresilon, Inc. — FDA 510(k) cleared unknown device.

Regulatory Information

Device ClassClass Class U
510(k) NumberK240713
Clearance Date2024-08-14
Clearance TypeTraditional
Product CodeQSY

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