Class Class II

V-VITFREEZE and V-VITWARM (K240176)

K240176 2024-09-13 Traditional
Home/ Devices/ V-VITFREEZE and V-VITWARM (K240176)

Description

V-VITFREEZE and V-VITWARM by Vitromed GmbH — FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240176
Clearance Date2024-09-13
Clearance TypeTraditional
Product CodeMQL
Regulation Number884.6180

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