V-PVP
K-Number: K232125 · 2024-03-20
Device Summary
Frequently Asked Questions
What is the V-PVP?
V-PVP is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Vitromed GmbH. The 510(k) number is K232125.
When did V-PVP receive FDA 510(k) clearance?
V-PVP received FDA 510(k) clearance on 2024-03-20, under 510(k) number K232125.
Who is the listed applicant for V-PVP?
The FDA 510(k) record lists Vitromed GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for V-PVP?
The FDA product code for V-PVP is MQL.
Other records listing Vitromed GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.