510(k) K000005
K000005 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE VALPROIC ACID, IMMULITE 2000 VALPROIC ACID, CATALOG # LKVA1, LKVA5 & L2KVA2, L2KVA6". The FDA issued a decision of Substantially Equivalent on March 3, 2000. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 3, 2000
- Date Received
- January 3, 2000
- 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