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Lumipulse G E2-III Calibrators

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163053
510(k) Type
Abbreviated
Applicant
Fujirebio Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2016
Days to Decision
30 days
Submission Type
Summary

Lumipulse G E2-III Calibrators

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163053
510(k) Type
Abbreviated
Applicant
Fujirebio Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2016
Days to Decision
30 days
Submission Type
Summary