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DRUGCHECK X MULTIDRUG SCREENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K992748
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1999
Days to Decision
17 days
Submission Type
Summary

DRUGCHECK X MULTIDRUG SCREENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K992748
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1999
Days to Decision
17 days
Submission Type
Summary