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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 K822065
Device Name KAM SUCKER
Applicant
THE ANSPACH EFFORT, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
THE ANSPACH EFFORT, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4800
Classification Product Code
KDC  
Date Received07/14/1982
Decision Date 08/16/1982
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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