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DUPONT ACA PLUS FSH/LH/PROLACTIN CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K941219
510(k) Type
Traditional
Applicant
DUPONT MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1994
Days to Decision
148 days
Submission Type
Summary

DUPONT ACA PLUS FSH/LH/PROLACTIN CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K941219
510(k) Type
Traditional
Applicant
DUPONT MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1994
Days to Decision
148 days
Submission Type
Summary