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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Blade, Scalpel
510(k) Number K884862
Device Name ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE
Applicant
ANCHOR PRODUCTS CO.
52 OFFICIAL RD.
ADDISON,  IL  60101
Applicant Contact ROBERT H THRUN
Correspondent
ANCHOR PRODUCTS CO.
52 OFFICIAL RD.
ADDISON,  IL  60101
Correspondent Contact ROBERT H THRUN
Regulation Number878.4800
Classification Product Code
GES  
Date Received11/21/1988
Decision Date 12/27/1988
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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