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IMMULITE ESTRADIOL

Page Type
Cleared 510(K)
510(k) Number
K932926
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1994
Days to Decision
209 days
Submission Type
Summary

IMMULITE ESTRADIOL

Page Type
Cleared 510(K)
510(k) Number
K932926
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1994
Days to Decision
209 days
Submission Type
Summary