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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 K822278
Device Name ENT FORCEPS
Applicant
KELLEHER CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
KELLEHER CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4800
Classification Product Code
GEN  
Date Received07/29/1982
Decision Date 08/27/1982
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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