Cleared Traditional

OB TRIPP TRANSPORT CHAIR

K830850 · Lic-Orthion · Physical Medicine
Apr 1983
Decision
19d
Days
Class 1
Risk

About This 510(k) Submission

K830850 is an FDA 510(k) clearance for the OB TRIPP TRANSPORT CHAIR, a Chair, With Casters (Class I — General Controls, product code INM), submitted by Lic-Orthion (Mchenry, US). The FDA issued a Cleared decision on April 5, 1983, 19 days after receiving the submission on March 17, 1983. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3100.

Submission Details

510(k) Number K830850 FDA.gov
FDA Decision Cleared SESE
Date Received March 17, 1983
Decision Date April 05, 1983
Days to Decision 19 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary —

Device Classification

Product Code INM — Chair, With Casters
Device Class Class I — General Controls
CFR Regulation 21 CFR 890.3100