Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K790018Substantially Equivalent

Serum, Potassium Determination of

Fisher Scientific Company L.L.C., Mchenry IL / Traditional, Substantially Equivalent

K790018 is the FDA 510(k) clearance record for SERUM, POTASSIUM DETERMINATION OF, a class II device, cleared for Fisher Scientific Co., LLC on under FDA product code CEM (Electrode, Ion Specific, Potassium). FDA records list 89 510(k) clearances for Fisher Scientific Co., LLC, from to . As of , FDA records show no recalls naming K790018.

Clearance record

Decision date
Received
(29 days to decision)
Product code
CEM Electrode, Ion Specific, Potassium
Regulation
21 CFR 862.1600
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Fisher Scientific Co., LLC 803 N. Front St. Suite 3, Mchenry IL
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