Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K932179Substantially Equivalent

Model 400/450 Electrolyte Analyzer

Ionetics, Inc., Costa Mesa CA / Traditional, Substantially Equivalent

K932179 is the FDA 510(k) clearance record for MODEL 400/450 ELECTROLYTE ANALYZER, a class II device, cleared for Ionetics, Inc. on under FDA product code JGS (Electrode, Ion Specific, Sodium). FDA records list 7 510(k) clearances for Ionetics, Inc., from to . As of , FDA records show no recalls naming K932179.

Clearance record

Decision date
Received
(196 days to decision)
Product code
JGS Electrode, Ion Specific, Sodium
Regulation
21 CFR 862.1665
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Ionetics, Inc. 3020 Enterprise, Costa Mesa CA
510(k) summary
Statement
Third party review
No

Clearances, product code JGS

Trailing 12 months
1 clearance under product code JGS in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JGS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260