V-PVP
K-Number: K232125 · 2024-03-20
ApplicantVitromed GmbH
Decision Date2024-03-20
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
V-PVP is a medical device manufactured by Vitromed GmbH. It received FDA 510(k) clearance on 2024-03-20 under approval number K232125. 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-PVP?
V-PVP is a medical device that received FDA 510(k) clearance on 2024-03-20. It is manufactured by Vitromed GmbH. The 510(k) number is K232125.
When was V-PVP approved by the FDA?
V-PVP received FDA 510(k) clearance on 2024-03-20, under approval number K232125.
What company makes V-PVP?
V-PVP is manufactured by Vitromed GmbH.
What is the FDA product code for V-PVP?
The FDA product code for V-PVP 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.