FDA 510(k) Application Details - K060235

Device Classification Name Enteroscope And Accessories

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510(K) Number K060235
Device Name Enteroscope And Accessories
Applicant SPIRUS MEDICAL, INC.
5 WHITCOMB AVENUE
AYER, MA 01432 US
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Contact PAMELA PAPINEAU
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Regulation Number 876.1500

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Classification Product Code FDA
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Date Received 01/30/2006
Decision Date 08/04/2006
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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