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ALBUMIN REAGENT SET

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832747
510(k) Type
Traditional
Applicant
BIORENT DIAGNOSTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1983
Days to Decision
60 days

ALBUMIN REAGENT SET

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832747
510(k) Type
Traditional
Applicant
BIORENT DIAGNOSTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1983
Days to Decision
60 days