VERDICT -II TCA, VERDICT-II MTD— 510(k) K011545
Substantially EquivalentMedtox Diagnostics, Inc.
FDA 510(k) clearance K011545 for VERDICT -II TCA, VERDICT-II MTD, Substantially Equivalent on 2001-06-08. Applicant: Medtox Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtox Diagnostics, Inc.
- Product code
- Code LFG
- Device class
- Class 2
- Regulation
- 21 CFR 862.3910
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Burlington, NC, US
Recent devices under product code LFG
view all- K151348 — Healgen Propoxyphene Test (Strip, Cassette, Cup, Dip Card), Healgen Nortriptyline Test (Strip, Cassette, Cup, Dip Card), Healgen EDDP (Methadone Metabolite) Test (Strip, Cassette, Cup, Dip Card)
- K142609 — CR3 Keyless Split Sample Cup Nortriptyline-Buprenorphine
- K112395 — WONDFO PHENCYCLIDINE URINE TEST, TRICYCLIC ANTIDEPRESSANTS URINE TEST
- K072062 — UCP MULTIPLE DRUG SCREEN TEST CUPS
- K061457 — UCP RAPID DRUG SCREENING TRICYCLIC ANTIDEPRESSANT, PROPOXYPHENE TESTS
More clearances from Medtox Diagnostics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.