FDA 510(k) Applications Submitted by GENICON, LC

FDA 510(k) Number Submission Date Device Name Applicant
K030269 01/27/2003 GENICON CLIP APPLIER GENICON, LC
K030174 01/17/2003 GENICON LAPAROSCOPES GENICON, LC
K991382 04/21/1999 SHIELDEDTROCAR/CANNULA SYSTEM, MODEL 101-005-101 GENICON, LC
K002542 08/16/2000 REUSABLE CANNULA GENICON, LC
K993625 10/26/1999 INSUFFLATION NEEDLE- 120MM, MODEL 900-200 GENICON, LC
K982472 07/15/1998 GENICON TROCAR GENICON, LC


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