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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name stents, drains and dilators for the biliary ducts
510(k) Number K861220
Device Name LUNDERQUIST - RING PTC DRAINAGE CATHETER
Applicant
MEADOX SURGIMED, INC.
112 BAUER DR.
OAKLAND,  NJ  07436
Applicant Contact JANE AOYAGI
Correspondent
MEADOX SURGIMED, INC.
112 BAUER DR.
OAKLAND,  NJ  07436
Correspondent Contact JANE AOYAGI
Regulation Number876.5010
Classification Product Code
FGE  
Date Received04/01/1986
Decision Date 05/19/1986
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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