FDA 510(k) Applications Submitted by Bioteque Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200103 | 01/17/2020 | BIOTEQ Drainage Catheter Set (One Step Type) | Bioteque Corporation |
| K210419 | 02/11/2021 | BIOTEQ Drainage Catheter BT-PDS-series | Bioteque Corporation |
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