FDA 510(k) Applications Submitted by OcuJect, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230372 | 02/13/2023 | VitreJect Syringe | OcuJect, LLC |
| K230959 | 04/04/2023 | VitreJect« Needle; OcuSafe« Needle | OcuJect, LLC |
| K212544 | 08/12/2021 | MiniLoad Syringe | OcuJect, LLC |
| K202432 | 08/25/2020 | MiniLoad Syringe | OcuJect, LLC |
| K170768 | 03/14/2017 | Mini Needle | OcuJect, LLC |
| K212805 | 09/02/2021 | SteriCap Mini Needle and Standard Needles | OcuJect, LLC |
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