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SteriCap Safety Needle; VitreJect Safety Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233343
510(k) Type
Abbreviated
Applicant
OcuJect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2023
Days to Decision
59 days
Submission Type
Summary

SteriCap Safety Needle; VitreJect Safety Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233343
510(k) Type
Abbreviated
Applicant
OcuJect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2023
Days to Decision
59 days
Submission Type
Summary