FDA 510(k) Application Details - K030170

Device Classification Name Endoscopic Tissue Approximation Device

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510(K) Number K030170
Device Name Endoscopic Tissue Approximation Device
Applicant OPUS MEDICAL, INC.
27127 CALLE ARROYO, SUITE 1924
SAN JUAN CAPISTRANO, CA 92675 US
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Contact JAMES W HART
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Regulation Number 876.1500

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Classification Product Code OCW
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Date Received 01/17/2003
Decision Date 07/28/2003
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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