VitreJect Syringe— 510(k) K230372
Substantially EquivalentOcuject, LLC
FDA 510(k) clearance K230372 for VitreJect Syringe, Substantially Equivalent on 2023-09-08. Applicant: Ocuject, LLC. Device class: 2.
Clearance details
- Applicant
- Ocuject, LLC
- Product code
- Code QLY
- Device class
- Class 2
- Regulation
- 21 CFR 880.5860
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newport Beach, CA, US
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More clearances from Ocuject, LLC
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