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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