FDA 510(k) Applications Submitted by Kevin Oh
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K010389 |
02/09/2001 |
CHAD THERAPEUTICS OXYMATIC MODEL 401 AND OXYMATIC MODEL 411 |
CHAD THERAPEUTICS, INC. |
K020475 |
02/12/2002 |
CHAD THERAPEUTICS OXYPENUMATIC CYPRESS MODEL 511 |
CHAD THERAPEUTICS, INC. |
K070740 |
03/16/2007 |
CHAD THERAPEUTICS BONSAI MODEL 800 |
CHAD THERAPEUTICS, INC. |
K081176 |
04/25/2008 |
FLOCHANNEL |
CHAD THERAPEUTICS, INC. |
K042142 |
08/09/2004 |
CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S |
CHAD THERAPEUTICS, INC. |
K013472 |
10/18/2001 |
TOTAL O2 |
CHAD THERAPEUTICS, INC. |
K033364 |
10/21/2003 |
CHAD THERAPEUTICS SAGE |
CHAD THERAPEUTICS, INC. |
K003455 |
11/07/2000 |
MODIFICATION TO CHAD THERAPEUTICS OXYMATIC MODEL 401 |
CHAD THERAPEUTICS, INC. |
K220239 |
01/28/2022 |
Solid State X-ray Imager(Model: FXRD-4386WB) |
Vieworks Co., Ltd. |
K221512 |
05/24/2022 |
Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW) |
Vieworks Co., Ltd. |
K210540 |
02/24/2021 |
Ohlendorf Clear Aligner |
Ohlendorf Appliance Laboratory |
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