510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033809Substantially Equivalent

Dimension Lidocaine (Lido) Flex Reagent Cartridge Method, Dimension Drug Calibrator II, Models Df113. Dc49d

Siemens Healthcare Diagnostics Inc., P.O. Box 6101, Newark DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033809 is the FDA 510(k) clearance record for DIMENSION LIDOCAINE (LIDO) FLEX REAGENT CARTRIDGE METHOD, DIMENSION DRUG CALIBRATOR II, MODELS DF113. DC49D, a class II device, cleared for Dade Behring, Inc. on under FDA product code KLR (Enzyme Immunoassay, Lidocaine). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K033809.

Clearance record

Decision date
Received
(74 days to decision)
Product code
KLR Enzyme Immunoassay, Lidocaine
Regulation
21 CFR 862.3555
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Dade Behring, Inc. Glasgow Business Community;, P.O. Box 6101, Newark DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KLR

Trailing 12 months

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

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