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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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