NEURAL STIMULATOR MONITOR— 510(k) K833809

Substantially Equivalent

Instromedix, Inc.

FDA 510(k) clearance K833809 for NEURAL STIMULATOR MONITOR, Substantially Equivalent on 1983-12-01. Applicant: Instromedix, Inc..

Clearance details

Applicant: Instromedix, Inc.
Product code: Code GZB
Advisory panel: Neurology
Date received: 1983-11-02
Decision date: 1983-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code GZB

product code GZB

Death: 4
Injury: 1,879
Other: 2
Total: 1,885

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.