Hangzhou Jimushi Meditech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Intermittent nelaton catheter for single use, Jimushi Sterile Urethral Catheter for single use
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hangzhou Jimushi Meditech Co., Ltd. Gastroenterology & Urology ✕
3 devices
Cleared
Jun 24, 2026
Hydrophilic coated intermittent nalaton catheter for single use-ready to use...
Gastroenterology & Urology
138d
Cleared
Apr 05, 2023
Intermittent nelaton catheter for single use
Gastroenterology & Urology
211d
Cleared
Jun 01, 2020
Jimushi Sterile Urethral Catheter for single use
Gastroenterology & Urology
132d