K020354

Substantially Equivalent

BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)

Applicant: Baylis Medical Co., Inc.
Product code: GXD
Advisory panel: Neurology
Date received: 2002-02-04
Decision date: 2002-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, Ontario, CA

Adverse events under product code GXD

product code GXD

Injury: 228
Total: 228

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.