FDA 510(k) Applications Submitted by ORTHOMERICA PRODUCTS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K090587 |
03/04/2009 |
STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K081994 |
07/14/2008 |
STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K082945 |
10/02/2008 |
STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K082950 |
10/03/2008 |
STARBAND |
ORTHOMERICA PRODUCTS, INC. |
K142141 |
08/05/2014 |
STARBAND, STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K141842 |
07/08/2014 |
STARBAND, STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K161138 |
04/22/2016 |
St. Louis Band |
ORTHOMERICA PRODUCTS, INC. |
K151147 |
04/30/2015 |
STARband, STARlight |
ORTHOMERICA PRODUCTS, INC. |
K151979 |
07/17/2015 |
STARband, STARlight |
ORTHOMERICA PRODUCTS, INC. |
K140353 |
02/12/2014 |
STARBAND AND STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K133250 |
10/22/2013 |
STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K124023 |
12/28/2012 |
STARBAND |
ORTHOMERICA PRODUCTS, INC. |
K021207 |
04/16/2002 |
STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
K021918 |
06/11/2002 |
CLARREN HELMET (ORTHOMERICA) |
ORTHOMERICA PRODUCTS, INC. |
K011350 |
05/02/2001 |
STARBAND CRANIAL ORTHOSIS |
ORTHOMERICA PRODUCTS, INC. |
K001167 |
04/10/2000 |
OPI BAND |
ORTHOMERICA PRODUCTS, INC. |
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