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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name sleeve, limb, compressible
510(k) Number K141390
Device Name INTERMITTENT PNEUMATIC COMPRESSION DEVICE
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,  CN 430206
Applicant Contact YAN LIU
Correspondent
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,  CN 430206
Correspondent Contact YAN LIU
Regulation Number870.5800
Classification Product Code
JOW  
Date Received05/27/2014
Decision Date 11/18/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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