510(k) K011164
K011164 is an FDA 510(k) premarket notification submitted by Syva Co., Dade Behring, Inc. for the device "MODIFICATION TO THE EMIT II PLUS METHAQUALONE ASSAY, MODEL OSR9Q229". The FDA issued a decision of Substantially Equivalent on May 10, 2001. The device falls under product code KXS (Radioimmunoassay, Methaqualone), a Class II device regulated under 21 CFR 862.3630. Syva Co., Dade Behring, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 10, 2001
- Date Received
- April 16, 2001
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Methaqualone
- Device Class
- Class II
- Regulation Number
- 862.3630
- Review Panel
- TX
- Submission Type