Cleared Traditional

RELIANCE MODEL 200 PODIATRY CHAIR

K860519 · F. & F. Koenigkramer · General Hospital
Feb 1986
Decision
8d
Days
Class 1
Risk

About This 510(k) Submission

K860519 is an FDA 510(k) clearance for the RELIANCE MODEL 200 PODIATRY CHAIR, a Table, Examination, Medical, Powered (Class I — General Controls, product code LGX), submitted by F. & F. Koenigkramer (Cincinnati, US). The FDA issued a Cleared decision on February 19, 1986, 8 days after receiving the submission on February 11, 1986. This device falls under the General Hospital review panel. Regulated under 21 CFR 878.4960.

Submission Details

510(k) Number K860519 FDA.gov
FDA Decision Cleared SESE
Date Received February 11, 1986
Decision Date February 19, 1986
Days to Decision 8 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary —

Device Classification

Product Code LGX — Table, Examination, Medical, Powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 878.4960