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QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043051
510(k) Type
Traditional
Applicant
PHAMATECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2005
Days to Decision
95 days
Submission Type
Summary

QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043051
510(k) Type
Traditional
Applicant
PHAMATECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2005
Days to Decision
95 days
Submission Type
Summary