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RAMP PROGESTURINE PDG ASSAY--48 TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860924
510(k) Type
Traditional
Applicant
MONOCLONAL ANTIBODIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1986
Days to Decision
113 days

RAMP PROGESTURINE PDG ASSAY--48 TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860924
510(k) Type
Traditional
Applicant
MONOCLONAL ANTIBODIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1986
Days to Decision
113 days