Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K933329Substantially Equivalent

King Diagnostics Iron and Total Iron Binding Capacity Reagent

King Diagnostics, Inc., Indianapolis IN / Traditional, Substantially Equivalent

K933329 is the FDA 510(k) clearance record for KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT, a class I device, cleared for King Diagnostics, Inc. on under FDA product code JMO (Ferrozine (Colorimetric) Iron Binding Capacity). FDA records list 41 510(k) clearances for King Diagnostics, Inc., from to . As of , FDA records show no recalls naming K933329.

Clearance record

Decision date
Received
(106 days to decision)
Product code
JMO Ferrozine (Colorimetric) Iron Binding Capacity
Regulation
21 CFR 862.1415
Device class
Class I
Review panel
Clinical Chemistry
Applicant
King Diagnostics, Inc. 6856 Hawthorn Park Dr., Indianapolis IN
510(k) summary
Statement
Third party review
No

Clearances, product code JMO

Trailing 12 months

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

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