FDA 510(k) Applications Submitted by Medicore Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212412 | 08/03/2021 | IRIS-XP | Medicore Co., Ltd. |
| K110374 | 02/09/2011 | MAX PULSE SYSTEM | MEDICORE CO., LTD. |
| K073323 | 11/27/2007 | SA-3000P | MEDICORE CO., LTD. |
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