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PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH

Page Type
Cleared 510(K)
510(k) Number
K873431
510(k) Type
Traditional
Applicant
SERONO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1987
Days to Decision
55 days

PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH

Page Type
Cleared 510(K)
510(k) Number
K873431
510(k) Type
Traditional
Applicant
SERONO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1987
Days to Decision
55 days