Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K904033Substantially Equivalent

Reflotron Potassium Test Tabs

Boehringer Mannheim Corp., Indianapolis IN / Traditional, Substantially Equivalent

K904033 is the FDA 510(k) clearance record for REFLOTRON POTASSIUM TEST TABS, a class II device, cleared for Boehringer Mannheim Corp. on under FDA product code CEJ (Tetraphenyl Borate, Colorimetry, Potassium). FDA records list 340 510(k) clearances for Boehringer Mannheim Corp., from to . As of , FDA records show no recalls naming K904033.

Clearance record

Decision date
Received
(67 days to decision)
Product code
CEJ Tetraphenyl Borate, Colorimetry, Potassium
Regulation
21 CFR 862.1600
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Boehringer Mannheim Corp. 9115 Hague Rd., Indianapolis IN
Third party review
No

Clearances, product code CEJ

Trailing 12 months

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

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