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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 K961891
Device Name WLP SINGLE-SEGMENT VERSION WLP SOLO VII
Applicant
WRIGHT LINEAR PUMP, INC.
408 NORTH TAYLOR AVE.
PITTSBURGH,  PA  15212
Applicant Contact JOE SORIERO
Correspondent
WRIGHT LINEAR PUMP, INC.
408 NORTH TAYLOR AVE.
PITTSBURGH,  PA  15212
Correspondent Contact JOE SORIERO
Regulation Number870.5800
Classification Product Code
JOW  
Date Received05/09/1996
Decision Date 11/06/1996
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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