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PROGESTERONE DIRECT RIA KIT-RADIOIMM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841333
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1984
Days to Decision
30 days

PROGESTERONE DIRECT RIA KIT-RADIOIMM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841333
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1984
Days to Decision
30 days