510(k) K983790

VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINE by Sun Biomedical Laboratories, Inc. — Product Code LCM

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