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IMMULITE PROLACTIN

Page Type
Cleared 510(K)
510(k) Number
K925846
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1993
Days to Decision
107 days
Submission Type
Statement

IMMULITE PROLACTIN

Page Type
Cleared 510(K)
510(k) Number
K925846
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1993
Days to Decision
107 days
Submission Type
Statement