A-LYTE® Integrated Multisensor (IMT Na K Cl)— 510(k) K222438

Name: FDA 510(k) clearance K222438
Creator: U.S. Food and Drug Administration
Published: 2023-07-25

Substantially Equivalent

Siemens Healthcare Diagnostics, Inc.

FDA 510(k) clearance K222438 for A-LYTE® Integrated Multisensor (IMT Na K Cl), Substantially Equivalent on 2023-07-25. Applicant: Siemens Healthcare Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Siemens Healthcare Diagnostics, Inc.
Product code: Code JGS
Device class: Class 2
Regulation: 21 CFR 862.1665
Advisory panel: Clinical Chemistry
Date received: 2022-08-12
Decision date: 2023-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, 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 →

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