FDA 510(k) Application Details - K142548

Device Classification Name Tubes, Gastrointestinal (And Accessories)

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510(K) Number K142548
Device Name Tubes, Gastrointestinal (And Accessories)
Applicant MEDICAL INNOVATION DEVELOPMENT
9, CHEMIN DU JUBIN
Dardilly FR
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Contact Melanie Fouilland
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Regulation Number 876.5980

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Classification Product Code KNT
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Date Received 09/10/2014
Decision Date 06/23/2015
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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