LXN FRUCTOSAMINE TEST— 510(k) K955629

Name: FDA 510(k) clearance K955629
Creator: U.S. Food and Drug Administration
Published: 1996-03-20

Substantially Equivalent

Lxn Corp.

FDA 510(k) clearance K955629 for LXN FRUCTOSAMINE TEST, Substantially Equivalent on 1996-03-20. Applicant: Lxn Corp.. Device class: 1.

Clearance details

Applicant: Lxn Corp.
Product code: Code JJX
Device class: Class 1
Regulation: 21 CFR 862.1660
Advisory panel: Clinical Chemistry
Date received: 1995-12-11
Decision date: 1996-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JJX

product code JJX

Other: 2
Total: 2

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 →

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