TWO RIVERS POWER LIFT/RECLINE CHAIR— 510(k) K991693

Name: FDA 510(k) clearance K991693
Creator: U.S. Food and Drug Administration
Published: 1999-08-17

Substantially Equivalent

Two Rivers, LLC

FDA 510(k) clearance K991693 for TWO RIVERS POWER LIFT/RECLINE CHAIR, Substantially Equivalent on 1999-08-17. Applicant: Two Rivers, LLC. Device class: 2.

Clearance details

Applicant: Two Rivers, LLC
Product code: Code INO
Device class: Class 2
Regulation: 21 CFR 890.3110
Advisory panel: Physical Medicine
Date received: 1999-05-18
Decision date: 1999-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Tazewell, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INO

view all

K131909 — DALTON LIFT CHAIR2014-02-24
K123834 — EASYSTAND BANTAM MEDIUM2013-08-13
K112944 — FRESENIUS MEDICAL TREATMENT CHAIR T688 SERIES2011-12-30
K101723 — COMPACT WHEELCHAIR PLATFORM2010-12-23
K091578 — LIFT CHAIR, MODEL T32009-12-02

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.