510(k) K011161
K011161 is an FDA 510(k) premarket notification submitted by Syva Co., Dade Behring, Inc. for the device "MODIFICATION TO THE EMIT II PLUS PHENCYCLIDINE ASSAY, MODEL OSR9J229". The FDA issued a decision of Substantially Equivalent on May 15, 2001. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. Syva Co., Dade Behring, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 15, 2001
- Date Received
- April 16, 2001
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Phencyclidine
- Device Class
- Class U
- Regulation Number
- Review Panel
- TX
- Submission Type