510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K011033Substantially Equivalent

Dimension Lithium (Li) Flex Reagent Cartridge, Model Df 132

Siemens Healthcare Diagnostics Inc., Newark DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K011033 is the FDA 510(k) clearance record for DIMENSION LITHIUM (LI) FLEX REAGENT CARTRIDGE, MODEL DF 132, a class II device, cleared for Dade Behring, Inc. on under FDA product code JIH (Flame Photometry, Lithium). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K011033.

Clearance record

Decision date
Received
(63 days to decision)
Product code
JIH Flame Photometry, Lithium
Regulation
21 CFR 862.3560
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Dade Behring, Inc. Glasgow Business Community, Newark DE
510(k) summary
Summary
Third party review
No

Clearances, product code JIH

Trailing 12 months

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

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