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

Page Type
Cleared 510(K)
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)
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