510(k) K014089

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

K014089 is an FDA 510(k) premarket notification submitted by Sun Biomedical Laboratories, Inc. for the device "VISUALINE II (ALSO KNOWN AS SUNLINE) BARITURATES". The FDA issued a decision of Substantially Equivalent on April 25, 2002. The device falls under product code DIS (Enzyme Immunoassay, Barbiturate), a Class II device regulated under 21 CFR 862.3150. Sun Biomedical Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 25, 2002
Date Received
December 11, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Barbiturate
Device Class
Class II
Regulation Number
862.3150
Review Panel
TX
Submission Type