V-PVP— 510(k) K232125

Substantially Equivalent

Vitromed GmbH

FDA 510(k) clearance K232125 for V-PVP, Substantially Equivalent on 2024-03-20. Applicant: Vitromed GmbH. Device class: 2.

Clearance details

Applicant: Vitromed GmbH
Product code: Code MQL
Device class: Class 2
Regulation: 21 CFR 884.6180
Advisory panel: Obstetrics/Gynecology
Date received: 2023-07-17
Decision date: 2024-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Langenfeld, DE

Download summary PDF View on FDA.gov ↗

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More clearances from Vitromed GmbH

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K222606 — V-HYADASE2023-05-26
K223117 — V-SPERM WASH2023-01-31
K193285 — V-ONESTEP2020-11-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.