LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle
FDA 510(k) clearance K242956 · decided 2024-10-25
Clearance details
- K-number
- K242956
- Device name
- LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle
- Applicant
- Ocuject, LLC
- Decision
- Substantially Equivalent
- Date received
- 2024-09-25
- Decision date
- 2024-10-25
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- QNS
- Device class
- 2
- Regulation number
- 880.5570
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Newport Beach, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| STERiJECT Low Dead Space, STERiJECT The Invisible Needle (K231734) | Tsk Laboratory International Japan KK | 2024-03-08 |
| EZ-Injec LDV Sterile Safety Needle (K210444) | Poonglim Pharmatech, Inc. | 2021-02-16 |
Recalls involving this device
No recalls on record reference this clearance.