FDA 510(k) Applications Submitted by DAVID C. KERR
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K141842 |
07/08/2014 |
STARBAND, STARLIGHT |
ORTHOMERICA PRODUCTS, INC. |
| K223238 |
10/20/2022 |
STARband 3D |
Orthomerica Products Inc. |
| K180109 |
01/16/2018 |
STARband, STARlight, St. Louis Band |
Orthomerica Products, Inc |
| K161138 |
04/22/2016 |
St. Louis Band |
ORTHOMERICA PRODUCTS, INC. |
| K151147 |
04/30/2015 |
STARband, STARlight |
ORTHOMERICA PRODUCTS, INC. |
| K211376 |
05/04/2021 |
STARband |
Orthomerica Products Inc. |
| K151979 |
07/17/2015 |
STARband, STARlight |
ORTHOMERICA PRODUCTS, INC. |
| K203098 |
10/14/2020 |
STARband, STARlight, St. Louis Band |
Orthomerica Products Inc. |
|
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