FDA 510(k) Applications Submitted by HRS Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132869 | 09/13/2013 | SILDENT | HRS CO., LTD. |
| K181604 | 06/19/2018 | Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite | HRS Co., Ltd. |
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