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ACON TRI-FECT DRUG SCREEN TEST DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041743
510(k) Type
Traditional
Applicant
Acon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2004
Days to Decision
73 days
Submission Type
Summary

ACON TRI-FECT DRUG SCREEN TEST DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041743
510(k) Type
Traditional
Applicant
Acon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2004
Days to Decision
73 days
Submission Type
Summary