FDA 510(k) Applications Submitted by GABRIEL KOROS

FDA 510(k) Number Submission Date Device Name Applicant
K120590 02/28/2012 DILATOR TUBE SET KOROS USA, INC.
K071338 05/14/2007 FLEX ARM RETRACTOR SYSTEM KOROS USA, INC.
K954016 08/25/1995 VIDEOSCOPE W/IRRIGATION SHEATH T. KOROS SURGICAL INSTRUMENTS CORP.


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