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IMMULITE TSH THIRD GENERATION CONTROL

Page Type
Cleared 510(K)
510(k) Number
K930007
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1993
Days to Decision
224 days
Submission Type
Statement

IMMULITE TSH THIRD GENERATION CONTROL

Page Type
Cleared 510(K)
510(k) Number
K930007
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1993
Days to Decision
224 days
Submission Type
Statement