FDA 510(k) Application Details - K192337

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K192337
Device Name	Sleeve, Limb, Compressible
Applicant	Dimedi Co., Ltd. 209ho, Wonju Venture Plaza, 130-2 Donghwagongdan-ro Munmak-eup Wonju-si 26365 KR Other 510(k) Applications for this Company
Contact	Nam Youn Other 510(k) Applications for this Contact
Regulation Number	870.5800   More FDA Info for this Regulation Number
Classification Product Code	JOW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/28/2019
Decision Date	06/22/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review