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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheter, peritoneal
510(k) Number K913733
Device Name STERILE CHEST TUBE
Applicant
VASCULAR PRODUCTS, INC.
P.O. BOX 2010
PALM HARBOR,  FL  34682
Applicant Contact PATRICK J LAMB
Correspondent
VASCULAR PRODUCTS, INC.
P.O. BOX 2010
PALM HARBOR,  FL  34682
Correspondent Contact PATRICK J LAMB
Regulation Number878.4200
Classification Product Code
GBW  
Date Received08/20/1991
Decision Date 10/08/1991
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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