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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cable, Electrode
510(k) Number K873361
Device Name LIFE-SPAN CABLE
Applicant
CHEMFET CORP.
777-108TH AVE. N.E. (1200)
RAINIER BANK PLAZA
BELLEVUE,  WA  98004
Applicant Contact LORI CADWELL
Correspondent
CHEMFET CORP.
777-108TH AVE. N.E. (1200)
RAINIER BANK PLAZA
BELLEVUE,  WA  98004
Correspondent Contact LORI CADWELL
Regulation Number890.1175
Classification Product Code
IKD  
Date Received08/21/1987
Decision Date 11/09/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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