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FDA 510(k) Applications Submitted by TRYLON CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K963391
08/28/1996
SPECULITE
TRYLON CORP.
K955790
12/22/1995
PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY
TRYLON CORP.
K011488
05/15/2001
SPIRABRUSH CX BIOPSY INSTRUMENT
TRYLON CORP.
K003995
12/26/2000
SPECULITE/ORALLITE
TRYLON CORP.
K012070
07/02/2001
ORALLITE COMPREHENSIVE EXAM TRAY
TRYLON CORP.
K033033
09/26/2003
VIZILITE-BLUE ORAL EXAM KIT
TRYLON CORP.
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