510(k) K024223

LIQUICHEK ANTI-RNP CONTROL, POSITIVE, CATALOG #116 by Bio-Rad — Product Code LKJ

K024223 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "LIQUICHEK ANTI-RNP CONTROL, POSITIVE, CATALOG #116". The FDA issued a decision of Substantially Equivalent on January 13, 2003. The device falls under product code LKJ (Antinuclear Antibody, Antigen, Control), a Class II device regulated under 21 CFR 866.5100. Bio-Rad has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 13, 2003
Date Received
December 23, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antinuclear Antibody, Antigen, Control
Device Class
Class II
Regulation Number
866.5100
Review Panel
IM
Submission Type