SYSTEM 90 AND 95— 510(k) K905293

Substantially Equivalent

Folio Products, Inc.

FDA 510(k) clearance K905293 for SYSTEM 90 AND 95, Substantially Equivalent on 1990-12-06. Applicant: Folio Products, Inc..

Clearance details

Applicant: Folio Products, Inc.
Product code: Code ITI
Advisory panel: Physical Medicine
Date received: 1990-11-23
Decision date: 1990-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Longmont, CO, US

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Adverse events under product code ITI

product code ITI

Death: 34
Injury: 778
Malfunction: 1,085
Other: 1
Total: 1,898

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.