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FDA 510(k) Applications Submitted by Fenlong Wu
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200134
01/21/2020
Jimushi Sterile Urethral Catheter for single use
Hangzhou Jimushi Meditech Co., Ltd.
K222677
09/06/2022
Intermittent nelaton catheter for single use
Hangzhou Jimushi Meditech Co., Ltd.
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