FDA 510(k) Applications Submitted by DyAnsys, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K071168 |
04/27/2007 |
THE PORTABLE ANSISCOPE |
DYANSYS, INC. |
| K173861 |
12/20/2017 |
Drug Relief |
DyAnsys, Inc. |
| K080036 |
01/07/2008 |
PORTABLE ECSCOPE 12I |
DYANSYS, INC. |
| K220397 |
02/11/2022 |
ANSiStim-PP |
DyAnsys, Inc. |
| K221231 |
04/29/2022 |
Drug Relief v1 |
DyAnsys, Inc. |
| K141168 |
05/06/2014 |
ANSISTIM |
DYANSYS, INC. |
| K091358 |
05/08/2009 |
ECSCOPE 100 |
DYANSYS, INC. |
| K091397 |
05/12/2009 |
ECSCOPE 200 |
DYANSYS, INC. |
| K221425 |
05/16/2022 |
Primary Relief |
DyAnsys, Inc. |
| K211971 |
06/24/2021 |
Drug Relief v1 |
DyAnsys, Inc. |
| K212859 |
09/08/2021 |
First Relief |
DyAnsys, Inc. |
| K213188 |
09/29/2021 |
Primary Relief |
DyAnsys, Inc. |
|
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