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REVISED LABELING FOR CANNABINOIDS TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K874269
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1987
Days to Decision
31 days

REVISED LABELING FOR CANNABINOIDS TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K874269
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1987
Days to Decision
31 days