DRUG TESTING ASSESSMENT PROGRAM QUALITY CONTROL

K913650 · Duo Research, Inc. · DIF · Sep 6, 1991 · Clinical Toxicology

Device Facts

Record IDK913650
Device NameDRUG TESTING ASSESSMENT PROGRAM QUALITY CONTROL
ApplicantDuo Research, Inc.
Product CodeDIF · Clinical Toxicology
Decision DateSep 6, 1991
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 862.3280
Device ClassClass 1

Regulatory Classification

Identification

A clinical toxicology control material is a device intended to provide an estimation of the precision of a device test system and to detect and monitor systematic deviations from accuracy resulting from reagent or instrument defects. This generic type of device includes various single, and multi-analyte control materials.

Innolitics

Panel 1

/
Ready

Predicate graph will load when search results are available.

Embedding visualization will load when search results are available.

PDF viewer will load when search results are available.

Loading panels...

Select an item from Submissions

Click any panel, subpart, regulation, product code, or device to see details here.

Section Matches

Results will appear here.

Product Code Matches

Results will appear here.

Special Control Matches

Results will appear here.

Loading collections...