510(k) K091884
K091884 is an FDA 510(k) premarket notification submitted by Ark Diagnostics, Inc. for the device "ARK ZONISAMIDE ASSAY, ARK ZONISAMIDE CALIBRATOR, AND ARK ZONISAMIDE CONTRO, MODELS 5022-0001-00, 5022-0002-00, 5022-0003". The FDA issued a decision of Substantially Equivalent on December 9, 2009. The device falls under product code NWM (Immunoassay, Anti-Seizure Drug), a Class II device regulated under 21 CFR 862.3350. Ark Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 9, 2009
- Date Received
- June 24, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Immunoassay, Anti-Seizure Drug
- Device Class
- Class II
- Regulation Number
- 862.3350
- Review Panel
- TX
- Submission Type
To aid in management of patients treated with anti-seizure drug.