V-GRAD
K-Number: K241833 · 2025-03-21
ApplicantVitromed GmbH
Decision Date2025-03-21
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
V-GRAD is a medical device manufactured by Vitromed GmbH. It received FDA 510(k) clearance on 2025-03-21 under approval number K241833. 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-GRAD?
V-GRAD is a medical device that received FDA 510(k) clearance on 2025-03-21. It is manufactured by Vitromed GmbH. The 510(k) number is K241833.
When was V-GRAD approved by the FDA?
V-GRAD received FDA 510(k) clearance on 2025-03-21, under approval number K241833.
What company makes V-GRAD?
V-GRAD is manufactured by Vitromed GmbH.
What is the FDA product code for V-GRAD?
The FDA product code for V-GRAD 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.