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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