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FDA 510(k)

Veress Needle

K-Number: K172120 · 2017-09-14

ApplicantWickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd
Decision Date2017-09-14
Product CodeFHO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Veress Needle is a medical device manufactured by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. It received FDA 510(k) clearance on 2017-09-14 under approval number K172120. The device is classified under product code FHO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Veress Needle?

Veress Needle is a medical device that received FDA 510(k) clearance on 2017-09-14. It is manufactured by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. The 510(k) number is K172120.

When was Veress Needle approved by the FDA?

Veress Needle received FDA 510(k) clearance on 2017-09-14, under approval number K172120.

What company makes Veress Needle?

Veress Needle is manufactured by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd.

What is the FDA product code for Veress Needle?

The FDA product code for Veress Needle is FHO.

Other Devices by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd

K172578Equipment Pouch K172794Suction Irrigation Set K172038Trocar K222828Specimen Bag, model: WEP040306B, WEP010304B, WEP040304B, WEP010759B, WEP010709B, WEP010304A, WEP010759A, WEP010709A K241022Sterile single use tip cleaner (WK800-S10 , WK800-S20)

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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