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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 K810338
Device Name LYMPHA PRESS
Applicant
MEGO AFEK
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
MEGO AFEK
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number870.5800
Classification Product Code
JOW  
Date Received02/09/1981
Decision Date 10/20/1981
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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