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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tray, surgical, instrument
510(k) Number K832137
Device Name CONVERTORS FLASH STERILIZING TRAY
Applicant
AMERICAN CONVERTORS DIV., AMERICAN PHARMASEAL
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
AMERICAN CONVERTORS DIV., AMERICAN PHARMASEAL
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4800
Classification Product Code
FSM  
Date Received07/01/1983
Decision Date 08/12/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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