Medical Device Manufacturer · CN , Hangzhou

Hangzhou Jimushi Meditech Co., Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2020

Recent clearances: Intermittent nelaton catheter for single use, Jimushi Sterile Urethral Catheter for single use

3
Total
3
Cleared
0
Denied

Hangzhou Jimushi Meditech Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Hangzhou, CN.

Latest FDA clearance: Jun 2026. Active since 2020. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Hangzhou Jimushi Meditech Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Vee Care (Asia) Limited as regulatory consultant.

FDA 510(k) Regulatory Record - Hangzhou Jimushi Meditech Co., Ltd.

3 devices
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