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TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000416
510(k) Type
Traditional
Applicant
Retinalabs.Com
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2000
Days to Decision
90 days
Submission Type
Summary

TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000416
510(k) Type
Traditional
Applicant
Retinalabs.Com
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2000
Days to Decision
90 days
Submission Type
Summary