FDA 510(k) Applications Submitted by LITECURE, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K070400 02/12/2007 LC THERAPY, MODEL LCT-1000 LITECURE, LLC
K173067 09/29/2017 LightForce LTS Model 1000, 1500, 2500, and 4000 LiteCure, LLC
K121487 05/18/2012 LITECURE THERAPY COMPACT LITECURE, LLC
K123014 09/27/2012 LITECURE THERAPY SYSTEM MODEL LTS-1500 LITECURE, LLC
K123031 09/28/2012 BWF-5 MEDICAL LASER SERIES LITECURE, LLC
K093087 10/01/2009 BWF-5 MEDICAL LASER SERIES LITECURE, LLC
K103511 11/30/2010 LITECURE THERAPY SYSTEM LITECURE, LLC


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