FDA 510(k) Applications Submitted by Chad Kugler
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K243691 | 11/26/2024 | LiquID .051 LP Guide Catheter Extension | Seigla Medical, Inc. |
| K220691 | 03/09/2022 | LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension | Seigla Medical, Inc. |
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