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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 K821906
Device Name CORPAK ENTERIC FEEDING TUBE W/GUIDE TIP
Applicant
CORPAK MEDSYSTEMS
1001 Asbury Dr
Buffalo Grove,  IL  60089
Applicant Contact Stephanie Wasielewski
Correspondent
CORPAK MEDSYSTEMS
1001 Asbury Dr
Buffalo Grove,  IL  60089
Correspondent Contact Stephanie Wasielewski
Regulation Number876.5980
Classification Product Code
KNT  
Date Received06/28/1982
Decision Date 07/13/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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