VERDICT II THC/COC/OPI/AMP, VERDICTII THC/COC/OPI,VERDICT II THC/COC/AMP,VERDICT II THC/COC/PCP,VERDICT II THC/COC— 510(k) K003687
Substantially EquivalentMedtox Diagnostics, Inc.
FDA 510(k) clearance K003687 for VERDICT II THC/COC/OPI/AMP, VERDICTII THC/COC/OPI,VERDICT II THC/COC/AMP,VERDICT II THC/COC/PCP,VERDICT II THC/COC, Substantially Equivalent on 2000-12-22. Applicant: Medtox Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtox Diagnostics, Inc.
- Product code
- Code DKE
- Device class
- Class 2
- Regulation
- 21 CFR 862.3870
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Burlington, NC, US
Recent devices under product code DKE
view all- K994405 — INSTANT-VIEW MARIJUANA URINE CASSETTE TEST
- K992068 — STATUS STIK, ACCUSIGN STIK
- K991751 — STATUS CUP ACCUSIGN CUP
- K991078 — ACCUSIGN DOA8, DOA8 PANEL, THC/OPI/COC/AMP/BZO/BAR/TCA/PCP, BIOSIGN DOA8, THC/OPI/COC/AMP/BZO/BAR/TCA/PAP, STATUS DS DO8
- K983147 — ACCUSIGN DOA 8, ACCUSIGN DOA 8 PANEL, ACCUSIGN THC/OPI/COC/AMP/BZO/BAR/TCA/PCP, BIOSIGN DOA 8, BIOSIGN THC/OPI/COC/AMP/P
More clearances from Medtox Diagnostics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.