510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K031231Substantially Equivalent

Liquicheck Urinalysis Control Bilevel, Model 435, Liquichek Urinalysis Control Level 2, Model 436, Liquichek Urinalysis

Bio-Rad, Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K031231 is the FDA 510(k) clearance record for LIQUICHECK URINALYSIS CONTROL BILEVEL, MODEL 435, LIQUICHEK URINALYSIS CONTROL LEVEL 2, MODEL 436, LIQUICHEK URINALYSIS, a class I device, cleared for Bio-Rad on under FDA product code JJW (Urinalysis Controls (Assayed And Unassayed)). FDA records list 319 510(k) clearances for Bio-Rad, from to . As of , FDA records show no recalls naming K031231.

Clearance record

Decision date
Received
(61 days to decision)
Product code
JJW Urinalysis Controls (Assayed And Unassayed)
Regulation
21 CFR 862.1660
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Bio-Rad 9500 Jeronimo Rd., Irvine CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JJW

Trailing 12 months

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

FDA records show no clearances under product code JJW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JJW, 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