FDA 510(k) Applications Submitted by Feeltech Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172602 | 08/30/2017 | Miracu | Feeltech Co., Ltd. |
| K213010 | 09/20/2021 | FEELject LDV (Low dead volume) syringe | Feeltech Co., Ltd. |
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