Last synced on 13 June 2025 at 11:06 pm

VitreJect Syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230372
510(k) Type
Traditional
Applicant
OcuJect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2023
Days to Decision
207 days
Submission Type
Summary

VitreJect Syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230372
510(k) Type
Traditional
Applicant
OcuJect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2023
Days to Decision
207 days
Submission Type
Summary