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IMMULITE PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K935138
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/1994
Days to Decision
75 days
Submission Type
Summary

IMMULITE PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K935138
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/1994
Days to Decision
75 days
Submission Type
Summary