Disposable Veress Needles
K-Number: K232401 · 2023-12-14
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.