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FDA 510(k) Application Details - K151471
Device Classification Name
Endoscopic Guidewire, Gastroenterology-Urology
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510(K) Number
K151471
Device Name
Endoscopic Guidewire, Gastroenterology-Urology
Applicant
Terumo Medical Corporation
265 Davidson Ave, Suite 320
Somerset, NJ 08873 US
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Contact
Phebe Varghese
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Regulation Number
876.1500
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Classification Product Code
OCY
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More FDA Info for this Product Code
Date Received
06/01/2015
Decision Date
09/17/2015
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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