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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name forceps, biopsy, non-electric
510(k) Number K946360
Device Name MODULAR BIOPSY FORCEP
Applicant
COX MEDICAL ENT., INC.
2186 EASTMAN AVE.
SUITE 110
VENTURA,  CA  93003
Applicant Contact LANITA COX
Correspondent
COX MEDICAL ENT., INC.
2186 EASTMAN AVE.
SUITE 110
VENTURA,  CA  93003
Correspondent Contact LANITA COX
Regulation Number876.1075
Classification Product Code
FCL  
Date Received12/30/1994
Decision Date 03/06/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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