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QUICKPROFILE SINGLE DRUG OF ABUSE DEVICE AND QUICK PROFILE MULTI-DRUGS OF ABUSE SCREEN DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130213
510(k) Type
Traditional
Applicant
LUMIQUICK DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2013
Days to Decision
262 days
Submission Type
Summary

QUICKPROFILE SINGLE DRUG OF ABUSE DEVICE AND QUICK PROFILE MULTI-DRUGS OF ABUSE SCREEN DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130213
510(k) Type
Traditional
Applicant
LUMIQUICK DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2013
Days to Decision
262 days
Submission Type
Summary