FDA 510(k) Application Details - K994087

Device Classification Name Endoscopic Tissue Approximation Device

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510(K) Number K994087
Device Name Endoscopic Tissue Approximation Device
Applicant SUTURA, INC.
17080 NEWHOPE ST.
FOUNTAIN VALLEY, CA 92708 US
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Contact DAVE BARRY
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Regulation Number 876.1500

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Classification Product Code OCW
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Date Received 12/03/1999
Decision Date 03/01/2000
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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