DIW — Hemagglutination Inhibition, Methadone Class II
FDA Device Classification
Classification Details
- Product Code
- DIW
- Device Class
- Class II
- Regulation Number
- 862.3620
- Submission Type
- Review Panel
- TX
- Medical Specialty
- Clinical Toxicology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K950182 | e.i. dupont de nemours and co | URINE METHADONE SCREEN FLEX(TM) REAGENT CARTRIDGE | March 21, 1995 |
| K930845 | roche diagnostic systems | ROCHE ABUSCREEN ONTRAK FOR METHADONE | April 20, 1993 |
| K801509 | technam | HI-M-TEST FOR METHADONE TEST #2 | July 14, 1980 |
| K760075 | j.t. baker chemical | KIT, METHADONE (TOXI-PAK IMMUNO HI) | July 20, 1976 |