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DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD

Page Type
Cleared 510(K)
510(k) Number
K943996
510(k) Type
Traditional
Applicant
DUPONT MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1994
Days to Decision
65 days
Submission Type
Summary

DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD

Page Type
Cleared 510(K)
510(k) Number
K943996
510(k) Type
Traditional
Applicant
DUPONT MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1994
Days to Decision
65 days
Submission Type
Summary