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QUICKSCREEN PRO MULTI DRUG SCREENING TEST , MODEL 9140-9147, 9061,9066, 9071, 9076, 9081 AND 9131

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980865
510(k) Type
Traditional
Applicant
PHAMATECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1998
Days to Decision
26 days
Submission Type
Statement

QUICKSCREEN PRO MULTI DRUG SCREENING TEST , MODEL 9140-9147, 9061,9066, 9071, 9076, 9081 AND 9131

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980865
510(k) Type
Traditional
Applicant
PHAMATECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1998
Days to Decision
26 days
Submission Type
Statement