MUSCLE DYSFUNCTION MONITOR— 510(k) K820568

Substantially Equivalent

A Company, Inc.

FDA 510(k) clearance K820568 for MUSCLE DYSFUNCTION MONITOR, Substantially Equivalent on 1982-04-09. Applicant: A Company, Inc..

Clearance details

Applicant: A Company, Inc.
Product code: Code DZM
Advisory panel: Dental
Date received: 1982-03-02
Decision date: 1982-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DZM

product code DZM

Injury: 139
Total: 139

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.