510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K014034Substantially Equivalent

Modification to Synchron Lx Clinical Chemistry Systems (Lx20 and Lx20 Pro)

Siemens Healthcare Diagnostics Inc., Brea CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K014034 is the FDA 510(k) clearance record for MODIFICATION TO SYNCHRON LX CLINICAL CHEMISTRY SYSTEMS (LX20 AND LX20 PRO), a class II device, cleared for Beckman Coulter, Inc. on under FDA product code JFL (Ph Rate Measurement, Carbon-Dioxide). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show 4 recalls naming K014034.

Clearance record

Decision date
Received
(11 days to decision)
Product code
JFL Ph Rate Measurement, Carbon-Dioxide
Regulation
21 CFR 862.1160
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Beckman Coulter, Inc. 200 S. Kraemer Blvd. W-110, Brea CA
510(k) summary
Summary
Third party review
No

Clearances, product code JFL

Trailing 12 months

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

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