510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K851234Substantially Equivalent

A-Just Turbidity Meter

Abbott Medical, Irving TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851234 is the FDA 510(k) clearance record for A-JUST TURBIDITY METER, a class I device, cleared for Abbott Laboratories on under FDA product code JQX (Nephelometer, For Clinical Use). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K851234.

Clearance record

Decision date
Received
(34 days to decision)
Product code
JQX Nephelometer, For Clinical Use
Regulation
21 CFR 862.2700
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Abbott Laboratories 1921 Hurd Dr., Irving TX
Third party review
No

Clearances, product code JQX

Trailing 12 months

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

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