CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000— 510(k) K990036

Name: FDA 510(k) clearance K990036
Creator: U.S. Food and Drug Administration
Published: 1999-03-18

Substantially Equivalent

Careside, Inc.

FDA 510(k) clearance K990036 for CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000, Substantially Equivalent on 1999-03-18. Applicant: Careside, Inc.. Device class: 2.

Clearance details

Applicant: Careside, Inc.
Product code: Product code JGS
Device class: Class 2
Regulation: 21 CFR 862.1665
Advisory panel: Clinical Chemistry
Date received: 1999-01-06
Decision date: 1999-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, 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 →

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