LCCS INSULATED SPINAL NEEDLE (RF CANNULA)— 510(k) K112231

Name: FDA 510(k) clearance K112231
Creator: U.S. Food and Drug Administration
Published: 2011-08-19

Substantially Equivalent

Lccs Products Limited

FDA 510(k) clearance K112231 for LCCS INSULATED SPINAL NEEDLE (RF CANNULA), Substantially Equivalent on 2011-08-19. Applicant: Lccs Products Limited. Device class: 2.

Clearance details

Applicant: Lccs Products Limited
Product code: Code GXI
Device class: Class 2
Regulation: 21 CFR 882.4725
Advisory panel: Neurology
Date received: 2011-08-04
Decision date: 2011-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, Guangdong, CN

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GXI

product code GXI

Death: 3
Injury: 171
Total: 174

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.