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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Pressure Applying
510(k) Number K780312
Device Name AUTONOM
Applicant
Autonomic Equipment Supply Co,
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Autonomic Equipment Supply Co,
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number890.5765
Classification Product Code
KNM  
Date Received02/15/1978
Decision Date 04/05/1978
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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