FDA 510(k) Applications Submitted by Joseph Howell
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170599 | 03/01/2017 | SureFlo EVD Catheter | Arkis BioSciences Inc. |
| K243186 | 09/30/2024 | Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (11364752); Symbia Pro.specta X7 (11364753); Symbia Pro.specta VA30A Family | Siemens Medical Solutions USA, Inc. |
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