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

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..

Clearance details

Applicant: Careside, Inc.
Product code: Code JGS
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 ↗

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.