Ocuject, LLC · Class II · Cleared Oct 25, 2024
| K-number | K242956 |
| Device name | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle |
| Applicant | Ocuject, LLC |
| Product code | QNS |
| Device class | Class II |
| Decision date | Oct 25, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 880.5570 |
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