510(k) K982880
K982880 is an FDA 510(k) premarket notification submitted by Dade Behring, Inc. for the device "DIMENSION(R) VALPROIC (VALP) ACID METHOD". The FDA issued a decision of Substantially Equivalent on August 25, 1998. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Dade Behring, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 25, 1998
- Date Received
- August 14, 1998
- 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