SYNCHRON LX I 725 CLINICAL SYSTEM— 510(k) K023049

Name: FDA 510(k) clearance K023049
Creator: U.S. Food and Drug Administration
Published: 2002-10-04

Substantially Equivalent

Beckman Coulter, Inc.

FDA 510(k) clearance K023049 for SYNCHRON LX I 725 CLINICAL SYSTEM, Substantially Equivalent on 2002-10-04. Applicant: Beckman Coulter, Inc.. Device class: 2.

Clearance details

Applicant: Beckman Coulter, Inc.
Product code: Code JGS
Device class: Class 2
Regulation: 21 CFR 862.1665
Advisory panel: Clinical Chemistry
Date received: 2002-09-12
Decision date: 2002-10-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JGS

product code JGS

Malfunction: 535
Total: 535

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K023049

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K023049.

Data sourced from openFDA. This site is unofficial and independent of the FDA.