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 the device name listed in this FDA 510(k) record. The listed applicant is Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. It received FDA 510(k) clearance on 2017-09-14 under 510(k) 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. The listed applicant is Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. The 510(k) number is K172120.

When did Veress Needle receive FDA 510(k) clearance?

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

Who is the listed applicant for Veress Needle?

The FDA 510(k) record lists Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Veress Needle?

The FDA product code for Veress Needle is FHO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.