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DUPONT DIMENSION AMYLASE METHOD

Page Type
Cleared 510(K)
510(k) Number
K942640
510(k) Type
Traditional
Applicant
DUPONT MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1994
Days to Decision
98 days
Submission Type
Summary

DUPONT DIMENSION AMYLASE METHOD

Page Type
Cleared 510(K)
510(k) Number
K942640
510(k) Type
Traditional
Applicant
DUPONT MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1994
Days to Decision
98 days
Submission Type
Summary