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RIA KIT, PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K782009
510(k) Type
Traditional
Applicant
THE UPJOHN CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1979
Days to Decision
91 days

RIA KIT, PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K782009
510(k) Type
Traditional
Applicant
THE UPJOHN CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1979
Days to Decision
91 days