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FDA 510(k)

Avantik VTM

K-Number: K233449 · 2024-07-15

ApplicantHanchang Medic Co., Ltd. (Han Chang Medic)
Decision Date2024-07-15
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Avantik VTM is the device name listed in this FDA 510(k) record. The listed applicant is Hanchang Medic Co., Ltd. (Han Chang Medic). It received FDA 510(k) clearance on 2024-07-15 under 510(k) 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. The listed applicant is Hanchang Medic Co., Ltd. (Han Chang Medic). The 510(k) number is K233449.

When did Avantik VTM receive FDA 510(k) clearance?

Avantik VTM received FDA 510(k) clearance on 2024-07-15, under 510(k) number K233449.

Who is the listed applicant for Avantik VTM?

The FDA 510(k) record lists Hanchang Medic Co., Ltd. (Han Chang Medic) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Avantik VTM?

The FDA product code for Avantik VTM is JSM.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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