510(k) K011528
K011528 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "EMIT 2000 PHENOBARBITAL ASSAY, MODEL OSR4D229". The FDA issued a decision of Substantially Equivalent on June 6, 2001. The device falls under product code DLZ (Enzyme Immunoassay, Phenobarbital), a Class II device regulated under 21 CFR 862.3660. Syva Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 2001
- Date Received
- May 17, 2001
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Phenobarbital
- Device Class
- Class II
- Regulation Number
- 862.3660
- Review Panel
- TX
- Submission Type