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FDA 510(k) Applications Submitted by LIFECELL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K052735
09/30/2005
ALLOCRAFT DBM
LIFECELL CORP.
K130817
03/25/2013
LTN - LAPAROSCOPIC SURGICAL MESH
LIFECELL CORP.
K112534
09/01/2011
LIFECELL TISSUE EXPANDER
LIFECELL CORP.
K080353
02/11/2008
LTM-T SURGICAL MESH
LIFECELL CORP.
K070560
02/27/2007
LRTM SURGICAL MESH
LIFECELL CORP.
K071986
07/20/2007
LTM-RC SURGICAL MESH
LIFECELL CORP.
K082176
08/01/2008
LTM-BPS SURGICAL MESH
LIFECELL CORP.
K082103
07/25/2008
LTM WOUND DRESSING
LIFECELL CORP.
K121289
04/30/2012
LTM-LABAROSCOPIC SURGICAL MESH
LIFECELL CORP.
K061208
05/01/2006
LIFECELL DURAL SUBSTITUTE MATRIX
LIFECELL CORP.
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