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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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