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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name instrument, surgical, disposable
510(k) Number K802485
Device Name SEARLE VASCULAR LOOPS
Applicant
G.D. SEARLE AND CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
G.D. SEARLE AND CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4800
Classification Product Code
KDC  
Date Received10/10/1980
Decision Date 02/12/1981
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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