510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902174Substantially Equivalent

Coulter Hdl - Cholesterol Reagent

Coulter Corp., Hialeah FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902174 is the FDA 510(k) clearance record for COULTER HDL - CHOLESTEROL REAGENT, a class I device, cleared for Coulter Corp. on under FDA product code LBR (Ldl & Vldl Precipitation, Hdl). FDA records list 51 510(k) clearances for Coulter Corp., from to . As of , FDA records show no recalls naming K902174.

Clearance record

Decision date
Received
(78 days to decision)
Product code
LBR Ldl & Vldl Precipitation, Hdl
Regulation
21 CFR 862.1475
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Coulter Corp. 745 W. 83rd St., Hialeah FL
Third party review
No

Clearances, product code LBR

Trailing 12 months

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

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