510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K121823Substantially Equivalent

Clinical Chloride Analyzer, Chloride Test System, Sweat Chloride Analyzer, Chloridometer, Chloride Coulometric

ELITechGroup Inc, Logan UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K121823 is the FDA 510(k) clearance record for CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRIC, a class II device, cleared for Wescor, Inc. on under FDA product code JFS (Coulometric, Chloride). FDA records list 32 510(k) clearances for ELITechGroup Inc, from to . As of , FDA records show no recalls naming K121823.

Clearance record

Decision date
Received
(279 days to decision)
Product code
JFS Coulometric, Chloride
Regulation
21 CFR 862.1170
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Wescor, Inc. 370 W 1700 S, Logan UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JFS

Trailing 12 months

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

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