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MODIFICATION TO KDI QUIK TEST MARIJUANA SCREEN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875219
510(k) Type
Traditional
Applicant
KEYSTONE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1988
Days to Decision
185 days

MODIFICATION TO KDI QUIK TEST MARIJUANA SCREEN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875219
510(k) Type
Traditional
Applicant
KEYSTONE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1988
Days to Decision
185 days