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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