GARELICK COMMODE— 510(k) K802511

Substantially Equivalent

Garelick Mfg. Co.

FDA 510(k) clearance K802511 for GARELICK COMMODE, Substantially Equivalent on 1980-11-12. Applicant: Garelick Mfg. Co..

Clearance details

Applicant: Garelick Mfg. Co.
Product code: Code ILS
Advisory panel: Physical Medicine
Date received: 1980-10-15
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code ILS

product code ILS

Death: 4
Injury: 200
Total: 204

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.