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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name catheter, ventricular, general & plastic surgery
510(k) Number K843906
Device Name SNYDER HEMOVAC WOUND DRAINAGE DEVICES
Applicant
SNYDER LABORATORIES, INC.
P.O. BOX 409
NEW PHILADELPHIA,  OH  44663 -
Applicant Contact KENNETH A HOFACKER
Correspondent
SNYDER LABORATORIES, INC.
P.O. BOX 409
NEW PHILADELPHIA,  OH  44663 -
Correspondent Contact KENNETH A HOFACKER
Regulation Number878.4200
Classification Product Code
GBS  
Date Received10/03/1984
Decision Date 11/05/1984
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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