510(k) K031032
K031032 is an FDA 510(k) premarket notification submitted by Medtox Diagnostics, Inc. for the device "VERDICT II, PROFILE II". The FDA issued a decision of Substantially Equivalent on July 14, 2003. The device falls under product code DJG (Enzyme Immunoassay, Opiates), a Class II device regulated under 21 CFR 862.3650. Medtox Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 14, 2003
- Date Received
- April 1, 2003
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Opiates
- Device Class
- Class II
- Regulation Number
- 862.3650
- Review Panel
- TX
- Submission Type