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FDA 510(k)

Single Use Bipolar Forceps

K-Number: K230432 · 2023-05-18

Decision Date2023-05-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Single Use Bipolar Forceps is a medical device manufactured by Hg Innovations, Ltd.. It received FDA 510(k) clearance on 2023-05-18 under approval number K230432. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single Use Bipolar Forceps?

Single Use Bipolar Forceps is a medical device that received FDA 510(k) clearance on 2023-05-18. It is manufactured by Hg Innovations, Ltd.. The 510(k) number is K230432.

When was Single Use Bipolar Forceps approved by the FDA?

Single Use Bipolar Forceps received FDA 510(k) clearance on 2023-05-18, under approval number K230432.

What company makes Single Use Bipolar Forceps?

Single Use Bipolar Forceps is manufactured by Hg Innovations, Ltd..

What is the FDA product code for Single Use Bipolar Forceps?

The FDA product code for Single Use Bipolar Forceps is GEI.

Related Clinical Trials

Other Devices by Hg Innovations, Ltd.

Related Devices (Code: GEI)

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.