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FDA 510(k)

Disposable Veress Needles

K-Number: K232401 · 2023-12-14

Decision Date2023-12-14
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Disposable Veress Needles is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Kangji Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-12-14 under 510(k) 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. The listed applicant is Hangzhou Kangji Medical Instrument Co., Ltd.. The 510(k) number is K232401.

When did Disposable Veress Needles receive FDA 510(k) clearance?

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

Who is the listed applicant for Disposable Veress Needles?

The FDA 510(k) record lists Hangzhou Kangji Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Veress Needles?

The FDA product code for Disposable Veress Needles is HIF.

Other records listing Hangzhou Kangji Medical Instrument 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.

Related Devices (Code: HIF)

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.

Official Source

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