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BIOSIGN(TM_ RUBELLA - RUBELLA ANTIBODY TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925355
510(k) Type
Traditional
Applicant
PRINCETON BIOMEDIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1994
Days to Decision
628 days
Submission Type
Statement

BIOSIGN(TM_ RUBELLA - RUBELLA ANTIBODY TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925355
510(k) Type
Traditional
Applicant
PRINCETON BIOMEDIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1994
Days to Decision
628 days
Submission Type
Statement