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FDA 510(k) Applications Submitted by Finemedix Co. Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K181690
06/26/2018
Clear-Jet Injection Catheter
Finemedix Co. Ltd.
K180363
02/09/2018
Clear-Tip EUS-FNA
Finemedix Co. Ltd.
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