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QUICK SCREEN BARBITURATE SCREENING TEST MODELS 9020 AND 9021, QUICK SCREEN PRO MULTI DRUG SCREENING TEST MODL 9152

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982152
510(k) Type
Traditional
Applicant
Phamatech
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1998
Days to Decision
95 days
Submission Type
Summary

QUICK SCREEN BARBITURATE SCREENING TEST MODELS 9020 AND 9021, QUICK SCREEN PRO MULTI DRUG SCREENING TEST MODL 9152

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982152
510(k) Type
Traditional
Applicant
Phamatech
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1998
Days to Decision
95 days
Submission Type
Summary