FDA 510(k) Applications Submitted by Kossel Medtech (Suzhou) Co.,Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231402 | 05/15/2023 | HP PTA Balloon Dilatation Catheter | Kossel Medtech (Suzhou) Co.,Ltd. |
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