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PROGESTERONE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K931228
510(k) Type
Traditional
Applicant
IMMUNOTECH CORP.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
10/22/1993
Days to Decision
226 days
Submission Type
Summary

PROGESTERONE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K931228
510(k) Type
Traditional
Applicant
IMMUNOTECH CORP.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
10/22/1993
Days to Decision
226 days
Submission Type
Summary