510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K890792Substantially Equivalent

Potassium and Sodium Electrolyte Analyzer

Ionetics, Inc., Costa Mesa CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890792 is the FDA 510(k) clearance record for POTASSIUM AND SODIUM ELECTROLYTE ANALYZER, a class II device, cleared for Ionetics, Inc. on under FDA product code CEM (Electrode, Ion Specific, Potassium). FDA records list 7 510(k) clearances for Ionetics, Inc., from to . As of , FDA records show no recalls naming K890792.

Clearance record

Decision date
Received
(75 days to decision)
Product code
CEM Electrode, Ion Specific, Potassium
Regulation
21 CFR 862.1600
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Ionetics, Inc. 3020 Enterprise, Costa Mesa CA
Third party review
No

Clearances, product code CEM

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