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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name forceps, general & plastic surgery
510(k) Number K821339
Device Name SALMONELLA POLY
Applicant
ANALYTICAL PRODUCTS, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
ANALYTICAL PRODUCTS, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4800
Classification Product Code
GEN  
Date Received05/05/1982
Decision Date 05/27/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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