Avantik VTM
K-Number: K233449 · 2024-07-15
Decision Date2024-07-15
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent
Device Summary
Avantik VTM is a medical device manufactured by Hanchang Medic Co., Ltd. (Han Chang Medic). It received FDA 510(k) clearance on 2024-07-15 under approval number K233449. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Avantik VTM?
Avantik VTM is a medical device that received FDA 510(k) clearance on 2024-07-15. It is manufactured by Hanchang Medic Co., Ltd. (Han Chang Medic). The 510(k) number is K233449.
When was Avantik VTM approved by the FDA?
Avantik VTM received FDA 510(k) clearance on 2024-07-15, under approval number K233449.
What company makes Avantik VTM?
Avantik VTM is manufactured by Hanchang Medic Co., Ltd. (Han Chang Medic).
What is the FDA product code for Avantik VTM?
The FDA product code for Avantik VTM is JSM.
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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.