510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873345Substantially Equivalent

'Microlyte 4/5'

Kone Instruments, Inc., Benseville IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873345 is the FDA 510(k) clearance record for 'MICROLYTE 4/5', a class II device, cleared for Kone Instruments, Inc. on under FDA product code JFP (Electrode, Ion Specific, Calcium). FDA records list 12 510(k) clearances for Kone Instruments, Inc., from to . As of , FDA records show no recalls naming K873345.

Clearance record

Decision date
Received
(23 days to decision)
Product code
JFP Electrode, Ion Specific, Calcium
Regulation
21 CFR 862.1145
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Kone Instruments, Inc. 1110 W. Throndale Ave., Benseville IL
Third party review
No

Clearances, product code JFP

Trailing 12 months

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

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