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PROGESTERONE DIRECT RIA KIT (125I)

Page Type
Cleared 510(K)
510(k) Number
K811907
510(k) Type
Traditional
Applicant
Immunalysis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1981
Days to Decision
22 days

PROGESTERONE DIRECT RIA KIT (125I)

Page Type
Cleared 510(K)
510(k) Number
K811907
510(k) Type
Traditional
Applicant
Immunalysis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1981
Days to Decision
22 days