Cleared Traditional

DALTON LIFT CHAIR

K131909 · Dalton Instrument Corp. · Physical Medicine
Feb 2014
Decision
243d
Days
Class 2
Risk

About This 510(k) Submission

K131909 is an FDA 510(k) clearance for the DALTON LIFT CHAIR, a Chair, Positioning, Electric (Class II — Special Controls, product code INO), submitted by Dalton Instrument Corp. (Addison, US). The FDA issued a Cleared decision on February 24, 2014, 243 days after receiving the submission on June 26, 2013. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3110.

Submission Details

510(k) Number K131909 FDA.gov
FDA Decision Cleared SESE
Date Received June 26, 2013
Decision Date February 24, 2014
Days to Decision 243 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

Device Classification

Product Code INO — Chair, Positioning, Electric
Device Class Class II — Special Controls
CFR Regulation 21 CFR 890.3110

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