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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name container, embedding
510(k) Number K831333
Device Name EMBEDDING RINGS
Applicant
SURGIPATH MEDICAL INDUSTRIES, INC.
MD 
Correspondent
SURGIPATH MEDICAL INDUSTRIES, INC.
MD 
Regulation Number864.3010
Classification Product Code
KER  
Date Received04/25/1983
Decision Date 05/25/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Pathology
510k Review Panel Pathology
Type Traditional
Reviewed by Third Party No
Combination Product No
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