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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 K991038
Device Name VASO PRESS DVT SYSTEM, MODELS VP500, VP501
Applicant
BRITT CORP., INC.
16 CREST DR.
COLTS NECK,  NJ  07722
Applicant Contact J. JAMES BRITTON
Correspondent
BRITT CORP., INC.
16 CREST DR.
COLTS NECK,  NJ  07722
Correspondent Contact J. JAMES BRITTON
Regulation Number870.5800
Classification Product Code
JOW  
Date Received03/29/1999
Decision Date 06/22/2000
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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