Hangzhou Jimushi Meditech Co., Ltd. FDA Approvals

0 new drug approvals and 2 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)510(k)Jun 24, 2026Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Jun 24, 2026
Intermittent nelaton catheter for single use510(k)Apr 5, 2023Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Apr 5, 2023