510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972609Substantially Equivalent

Variant Express Glycohemoglobin Program

Bio-Rad, Hercules CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972609 is the FDA 510(k) clearance record for VARIANT EXPRESS GLYCOHEMOGLOBIN PROGRAM, a class II device, cleared for Bio-Rad on under FDA product code LCQ (Fluorescent Immunoassay Gentamicin). FDA records list 319 510(k) clearances for Bio-Rad, from to . As of , FDA records show no recalls naming K972609.

Clearance record

Decision date
Received
(26 days to decision)
Product code
LCQ Fluorescent Immunoassay Gentamicin
Regulation
21 CFR 862.3450
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Bio-Rad 4000 Alfred Nobel Dr., Hercules CA
510(k) summary
Summary
Third party review
No

Clearances, product code LCQ

Trailing 12 months

FDA records hold no clearances under product code LCQ in the trailing twelve months.

FDA records show no clearances under product code LCQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LCQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260