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FDA 510(k)

Disposable Veress Needles

K-Number: K232401 · 2023-12-14

ApplicantHangzhou Kangji Medical Instrument Co., Ltd.
Decision Date2023-12-14
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Disposable Veress Needles is a medical device manufactured by Hangzhou Kangji Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-12-14 under approval number K232401. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Veress Needles?

Disposable Veress Needles is a medical device that received FDA 510(k) clearance on 2023-12-14. It is manufactured by Hangzhou Kangji Medical Instrument Co., Ltd.. The 510(k) number is K232401.

When was Disposable Veress Needles approved by the FDA?

Disposable Veress Needles received FDA 510(k) clearance on 2023-12-14, under approval number K232401.

What company makes Disposable Veress Needles?

Disposable Veress Needles is manufactured by Hangzhou Kangji Medical Instrument Co., Ltd..

What is the FDA product code for Disposable Veress Needles?

The FDA product code for Disposable Veress Needles is HIF.

Other Devices by Hangzhou Kangji Medical Instrument Co., Ltd.

K233263Disposable Trocars K250643Disposable Polymer Ligation Clips

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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.

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