FDA 510(k) Application Details - K141390

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K141390
Device Name	Sleeve, Limb, Compressible
Applicant	WUHAN LANDING MEDICAL HI-TECH LTD 818 GAOXIN RD EAST LAKE HIGH TECH DEVELOPMENT ZONE FLOORS 1&2,UNITS B&C&D BUILDING NO.B7 MED EQUIPMENT PK WUHAM 430206 CN Other 510(k) Applications for this Company
Contact	YAN LIU 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	05/27/2014
Decision Date	11/18/2014
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