ClearGrasp Snare
K-Number: K183289 · 2019-03-06
ApplicantFinemedix Co., Ltd.
Decision Date2019-03-06
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
ClearGrasp Snare is a medical device manufactured by Finemedix Co., Ltd.. It received FDA 510(k) clearance on 2019-03-06 under approval number K183289. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ClearGrasp Snare?
ClearGrasp Snare is a medical device that received FDA 510(k) clearance on 2019-03-06. It is manufactured by Finemedix Co., Ltd.. The 510(k) number is K183289.
When was ClearGrasp Snare approved by the FDA?
ClearGrasp Snare received FDA 510(k) clearance on 2019-03-06, under approval number K183289.
What company makes ClearGrasp Snare?
ClearGrasp Snare is manufactured by Finemedix Co., Ltd..
What is the FDA product code for ClearGrasp Snare?
The FDA product code for ClearGrasp Snare is FDI.
Other Devices by Finemedix 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.