Disposable Bipolar Forceps
K-Number: K232703 · 2024-03-06
Decision Date2024-03-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Disposable Bipolar Forceps is a medical device manufactured by Jiangsu Hope Biomedical Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-03-06 under approval number K232703. 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 Disposable Bipolar Forceps?
Disposable Bipolar Forceps is a medical device that received FDA 510(k) clearance on 2024-03-06. It is manufactured by Jiangsu Hope Biomedical Science & Technology Co., Ltd.. The 510(k) number is K232703.
When was Disposable Bipolar Forceps approved by the FDA?
Disposable Bipolar Forceps received FDA 510(k) clearance on 2024-03-06, under approval number K232703.
What company makes Disposable Bipolar Forceps?
Disposable Bipolar Forceps is manufactured by Jiangsu Hope Biomedical Science & Technology Co., Ltd..
What is the FDA product code for Disposable Bipolar Forceps?
The FDA product code for Disposable Bipolar Forceps is GEI.
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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.