FDA 510(k) Applications Submitted by Stimwave Technologies Inc.,DBA StimQ LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171366 | 05/09/2017 | Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit | Stimwave Technologies Inc.,DBA StimQ LLC |
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