SERIES 9000 LIFT-RECLINE CHAIR— 510(k) K903905

Substantially Equivalent

Equi-Tron Mfg., Inc.

FDA 510(k) clearance K903905 for SERIES 9000 LIFT-RECLINE CHAIR, Substantially Equivalent on 1990-09-17. Applicant: Equi-Tron Mfg., Inc..

Clearance details

Applicant: Equi-Tron Mfg., Inc.
Product code: Code INO
Advisory panel: Physical Medicine
Date received: 1990-08-23
Decision date: 1990-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Niagara Falls, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code INO

product code INO

Death: 6
Total: 6

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.