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IMMULITE TOTAL TESTOSTERONE

Page Type
Cleared 510(K)
510(k) Number
K955870
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1996
Days to Decision
40 days
Submission Type
Summary

IMMULITE TOTAL TESTOSTERONE

Page Type
Cleared 510(K)
510(k) Number
K955870
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1996
Days to Decision
40 days
Submission Type
Summary