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IMMULITE PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K944211
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1994
Days to Decision
112 days
Submission Type
Statement

IMMULITE PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K944211
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1994
Days to Decision
112 days
Submission Type
Statement