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FDA 510(k)

Victan

K-Number: K230593 · 2023-05-30

ApplicantJiangsu Haize Medical Scientific Development Co., Ltd.
Decision Date2023-05-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Victan is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Haize Medical Scientific Development Co., Ltd.. It received FDA 510(k) clearance on 2023-05-30 under 510(k) number K230593. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Victan?

Victan is a medical device that received FDA 510(k) clearance on 2023-05-30. The listed applicant is Jiangsu Haize Medical Scientific Development Co., Ltd.. The 510(k) number is K230593.

When did Victan receive FDA 510(k) clearance?

Victan received FDA 510(k) clearance on 2023-05-30, under 510(k) number K230593.

Who is the listed applicant for Victan?

The FDA 510(k) record lists Jiangsu Haize Medical Scientific Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Victan?

The FDA product code for Victan is GEI.

Other records listing Jiangsu Haize Medical Scientific Development Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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