510(k) K983790
K983790 is an FDA 510(k) premarket notification submitted by Sun Biomedical Laboratories, Inc. for the device "VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINE". The FDA issued a decision of Substantially Equivalent on March 1, 1999. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. Sun Biomedical Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 1, 1999
- Date Received
- October 27, 1998
- Clearance Type
- Traditional
- 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