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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 K930526
Device Name INTERMITTENT COMPRESSION SYSTEM MODEL 5000
Applicant
ADVANCED INSTRUMENTS, INC.
TOW TECHNOLOGY WAY
NORWOOD,  MA  02062
Applicant Contact DOUGLAS GUERETTE
Correspondent
ADVANCED INSTRUMENTS, INC.
TOW TECHNOLOGY WAY
NORWOOD,  MA  02062
Correspondent Contact DOUGLAS GUERETTE
Regulation Number870.5800
Classification Product Code
JOW  
Date Received02/02/1993
Decision Date 11/18/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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