Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K802080Substantially Equivalent

Baker Diag. Ultrarate Chloride Kit

J.T. Baker Chemical Co., Mchenry IL / Traditional, Substantially Equivalent

K802080 is the FDA 510(k) clearance record for BAKER DIAG. ULTRARATE CHLORIDE KIT, a class II device, cleared for J.T. Baker Chemical Co. on under FDA product code JFS (Coulometric, Chloride). FDA records list 54 510(k) clearances for J.T. Baker Chemical Co., from to . As of , FDA records show no recalls naming K802080.

Clearance record

Decision date
Received
(43 days to decision)
Product code
JFS Coulometric, Chloride
Regulation
21 CFR 862.1170
Device class
Class II
Review panel
Clinical Chemistry
Applicant
J.T. Baker Chemical Co. 803 N. Front St. Suite 3, Mchenry IL
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