FDA 510(k) Application Details - K110653

Device Classification Name Catheter, Straight

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510(K) Number K110653
Device Name Catheter, Straight
Applicant CURE MEDICAL LLC.
3722 AVENUE SAUSALITO
IRVINE, CA 92606 US
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Contact ROBYN SCOPIS
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Regulation Number 876.5130

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Classification Product Code EZD
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Date Received 03/07/2011
Decision Date 08/01/2011
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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