K-number	K240176
Device name	V-VITFREEZE and V-VITWARM
Applicant	Vitromed GmbH
Product code	MQL
Device class	Class II
Decision date	Sep 13, 2024
Decision	Substantially Equivalent
Regulation	884.6180

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View the full FDA submission: accessdata.fda.gov

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V-VITFREEZE and V-VITWARM

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