510(k) K972609

VARIANT EXPRESS GLYCOHEMOGLOBIN PROGRAM by Bio-Rad — Product Code LCQ

K972609 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "VARIANT EXPRESS GLYCOHEMOGLOBIN PROGRAM". The FDA issued a decision of Substantially Equivalent on August 6, 1997. The device falls under product code LCQ (Fluorescent Immunoassay Gentamicin), a Class II device regulated under 21 CFR 862.3450. Bio-Rad has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 6, 1997
Date Received
July 11, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fluorescent Immunoassay Gentamicin
Device Class
Class II
Regulation Number
862.3450
Review Panel
TX
Submission Type