510(k) K032049
K032049 is an FDA 510(k) premarket notification submitted by Roche Diagnostics Corp. for the device "ROCHE ONLINE TDM VALPROIC ACID". The FDA issued a decision of Substantially Equivalent on August 22, 2003. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Roche Diagnostics Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 22, 2003
- Date Received
- July 2, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Valproic Acid
- Device Class
- Class II
- Regulation Number
- 862.3645
- Review Panel
- TX
- Submission Type