Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact