FDA 510(k) Applications for Medical Device Product Code: KXP (Stent, Vaginal)

FDA 510(k) Applications for Medical Device Product Code "KXP"
(Stent, Vaginal)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K983045	Owen Mumford USA, Inc.	AMIELLE	11/25/1998
K202542	PMT Corporation	Allura Vaginal Stent	09/30/2020
K974479	SILIMED, LLC.	SILIMED VAGINAL STENT	08/05/1998

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