Single Use Bipolar Forceps
K-Number: K230432 · 2023-05-18
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.