KLS MARTIN QUICK DISC— 510(k) K062857

Substantially Equivalent

KLS Martin L.P.

FDA 510(k) clearance K062857 for KLS MARTIN QUICK DISC, Substantially Equivalent on 2006-11-22. Applicant: KLS Martin L.P..

Clearance details

Applicant: KLS Martin L.P.
Product code: Code GXN
Advisory panel: Neurology
Date received: 2006-09-25
Decision date: 2006-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

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Adverse events under product code GXN

product code GXN

Injury: 208
Total: 208

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.