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Lumipulse G B•R•A•H•M•S PCT Immunoreaction Cartridges, Lumipulse G B•R•A•H•M•S PCT Calibrators set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172713
510(k) Type
Traditional
Applicant
Fujirebio Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2017
Days to Decision
93 days
Submission Type
Summary

Lumipulse G B•R•A•H•M•S PCT Immunoreaction Cartridges, Lumipulse G B•R•A•H•M•S PCT Calibrators set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172713
510(k) Type
Traditional
Applicant
Fujirebio Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2017
Days to Decision
93 days
Submission Type
Summary