Trocar
K-Number: K172038 · 2017-10-27
Decision Date2017-10-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Trocar is a medical device manufactured by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. It received FDA 510(k) clearance on 2017-10-27 under approval number K172038. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Trocar?
Trocar is a medical device that received FDA 510(k) clearance on 2017-10-27. It is manufactured by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. The 510(k) number is K172038.
When was Trocar approved by the FDA?
Trocar received FDA 510(k) clearance on 2017-10-27, under approval number K172038.
What company makes Trocar?
Trocar is manufactured by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd.
What is the FDA product code for Trocar?
The FDA product code for Trocar is GCJ.
Other Devices by Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd
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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.