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BIOGENEX MONOCLONAL ANTI-PROGESTERONE RECEPTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012960
510(k) Type
Traditional
Applicant
Biogenex Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2002
Days to Decision
185 days
Submission Type
Summary

BIOGENEX MONOCLONAL ANTI-PROGESTERONE RECEPTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012960
510(k) Type
Traditional
Applicant
Biogenex Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2002
Days to Decision
185 days
Submission Type
Summary