Comprehensive Test Menu

ToxLok Validity Test

 

Insource Diagnostics

ToxLok Validity Test

Test Code: 16101

CPT: None
Tests Included ToxLok Validity Test
Use Compliance Monitoring
Clinical Utility Determine therapeutic use, abuse, diversion
Intended Patient Population Any 
Patient Preparation None
Sample Buccal + Urine
Collection Device Swab + Urine Cup or Monovette
Sample Volume 1 Swab + 60mL of Urine
Min Sample Volume 1 Swab + 10mL
Test Methodology PCR & MALDI-TOF
Test Turnaround Time 7 Days
Limitations None
Shipping Ambient
Specimen Stability 14 Days RT but should be received in 7 Days
Laboratory Developed Test (LDT) Yes
CMS Guidance None
References None