V-HYADASE
K-Number: K222606 · 2023-05-26
ApplicantVitromed GmbH
Decision Date2023-05-26
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
V-HYADASE is a medical device manufactured by Vitromed GmbH. It received FDA 510(k) clearance on 2023-05-26 under approval number K222606. 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-HYADASE?
V-HYADASE is a medical device that received FDA 510(k) clearance on 2023-05-26. It is manufactured by Vitromed GmbH. The 510(k) number is K222606.
When was V-HYADASE approved by the FDA?
V-HYADASE received FDA 510(k) clearance on 2023-05-26, under approval number K222606.
What company makes V-HYADASE?
V-HYADASE is manufactured by Vitromed GmbH.
What is the FDA product code for V-HYADASE?
The FDA product code for V-HYADASE 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.