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SteriCap Mini Needle and Standard Needles

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212805
510(k) Type
Special
Applicant
OcuJect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2021
Days to Decision
28 days
Submission Type
Summary

SteriCap Mini Needle and Standard Needles

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212805
510(k) Type
Special
Applicant
OcuJect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2021
Days to Decision
28 days
Submission Type
Summary