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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tubes, gastrointestinal (and accessories)
510(k) Number K090559
Device Name FOOTPRINT MEDICAL SILICONE FEEDING TUBE
Applicant
FOOTPRINT MEDICAL
1203 CAMDEN ST.
SAN ANTONIO,  TX  78215
Applicant Contact CLYDE BAKER
Correspondent
FOOTPRINT MEDICAL
1203 CAMDEN ST.
SAN ANTONIO,  TX  78215
Correspondent Contact CLYDE BAKER
Regulation Number876.5980
Classification Product Code
KNT  
Date Received03/02/2009
Decision Date 05/04/2009
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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