LADD MEDICAL S-2000— 510(k) K862012

Substantially Equivalent

Ladd Research Industries, Inc.

FDA 510(k) clearance K862012 for LADD MEDICAL S-2000, Substantially Equivalent on 1986-06-09. Applicant: Ladd Research Industries, Inc..

Clearance details

Applicant: Ladd Research Industries, Inc.
Product code: Code GWM
Advisory panel: Neurology
Date received: 1986-05-28
Decision date: 1986-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, VT, US

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Adverse events under product code GWM

product code GWM

Death: 21
Injury: 732
Malfunction: 2,063
Other: 1
Total: 2,817

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.