ClearTip
K-Number: K231267 · 2023-06-30
ApplicantFinemedix Co., Ltd.
Decision Date2023-06-30
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
ClearTip is a medical device manufactured by Finemedix Co., Ltd.. It received FDA 510(k) clearance on 2023-06-30 under approval number K231267. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ClearTip?
ClearTip is a medical device that received FDA 510(k) clearance on 2023-06-30. It is manufactured by Finemedix Co., Ltd.. The 510(k) number is K231267.
When was ClearTip approved by the FDA?
ClearTip received FDA 510(k) clearance on 2023-06-30, under approval number K231267.
What company makes ClearTip?
ClearTip is manufactured by Finemedix Co., Ltd..
What is the FDA product code for ClearTip?
The FDA product code for ClearTip is FCG.
Other Devices by Finemedix Co., Ltd.
Related Devices (Code: FCG)
K160423Perineologic Access NeedleCorbin Clinical Resources, LLC
K160098Single Use Aspiration Needle NA-U401SXOlympus Medical Systems Corp.
K160229Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy NeedleCook Ireland, Ltd.
K171956Sterile Endoscope Biopsy Sampling NeedleChangzhou Detain Medical Devices Co., Ltd.
K171596ECHO-3-22: Echotip Ultra and EUSN-1, EUSN-3: Echotip Ultrasound NeedleWilson-Cook Medical, Inc.
K160890Howell Biliary Introducer NeedleWilson-Cook Medical, Inc.
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.