FDA 510(k) Applications Submitted by LifeCell Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K162752 09/30/2016 ARTIA Reconstructive Tissue Matrix Perforated LIFECELL CORPORATION
K163647 12/23/2016 Revolve Envi 600 Advanced Adipose System LifeCell Corporation
K193539 12/20/2019 REVOLVE ENVI 600 Advanced Adipose System LifeCell Corporation
K150712 03/19/2015 LTM-Perforated Surgical Mesh LifeCell Corporation
K142326 08/20/2014 HP Tissue Matrix LifeCell Corporation


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