Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Jiangsu Haize Medical Scientific Development Co., Ltd.. It received FDA 510(k) clearance on 2023-05-30 under approval 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. It is manufactured by Jiangsu Haize Medical Scientific Development Co., Ltd.. The 510(k) number is K230593.

When was Victan approved by the FDA?

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

What company makes Victan?

Victan is manufactured by Jiangsu Haize Medical Scientific Development Co., Ltd..

What is the FDA product code for Victan?

The FDA product code for Victan is GEI.

Other Devices by Jiangsu Haize Medical Scientific Development Co., Ltd.

K161421Single Use Surgical Suction Irrigator

Related Devices (Code: GEI)

K161307NICO MyriadNico Corporation K163190InMode RF SystemInmode MD , Ltd. K163373PK AIMGyrus Acmi, Inc. K163106CODMAN Integrated Bipolar Cord and Tubing SetMedos International SARL K162676Voyant Open Fusion DeviceApplied Medical Resources K162941Ligasure Blunt Tip, Sealer/Divider, Nano-coatedCovidien

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.

↑