V-VITFREEZE and V-VITWARM
K-Number: K240176 · 2024-09-13
ApplicantVitromed GmbH
Decision Date2024-09-13
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
V-VITFREEZE and V-VITWARM is a medical device manufactured by Vitromed GmbH. It received FDA 510(k) clearance on 2024-09-13 under approval number K240176. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the V-VITFREEZE and V-VITWARM?
V-VITFREEZE and V-VITWARM is a medical device that received FDA 510(k) clearance on 2024-09-13. It is manufactured by Vitromed GmbH. The 510(k) number is K240176.
When was V-VITFREEZE and V-VITWARM approved by the FDA?
V-VITFREEZE and V-VITWARM received FDA 510(k) clearance on 2024-09-13, under approval number K240176.
What company makes V-VITFREEZE and V-VITWARM?
V-VITFREEZE and V-VITWARM is manufactured by Vitromed GmbH.
What is the FDA product code for V-VITFREEZE and V-VITWARM?
The FDA product code for V-VITFREEZE and V-VITWARM is MQL.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.