510(k) K984396

LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213 by Bio-Rad — Product Code LRM

K984396 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213". The FDA issued a decision of Substantially Equivalent on December 18, 1998. The device falls under product code LRM (Anti-Dna Antibody (Enzyme-Labeled), 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
December 18, 1998
Date Received
December 9, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control
Device Class
Class II
Regulation Number
866.5100
Review Panel
IM
Submission Type