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Lumipulse G ß-Amyloid Ratio (1-42/1-40)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN200072
510(k) Type
Direct
Applicant
Fujirebio Diagnostics, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
5/4/2022
Days to Decision
530 days

Lumipulse G ß-Amyloid Ratio (1-42/1-40)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN200072
510(k) Type
Direct
Applicant
Fujirebio Diagnostics, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
5/4/2022
Days to Decision
530 days