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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Examination, Medical, Powered
510(k) Number K830294
Device Name MEDICAL EXAM TABLE
Applicant
Coe Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Coe Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number878.4960
Classification Product Code
LGX  
Date Received01/27/1983
Decision Date 01/11/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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