ORBITER(TM) TREADMILL— 510(k) K897179

Name: FDA 510(k) clearance K897179
Creator: U.S. Food and Drug Administration
Published: 1990-02-15

Substantially Equivalent

Lee-Meredith Industries, Inc.

FDA 510(k) clearance K897179 for ORBITER(TM) TREADMILL, Substantially Equivalent on 1990-02-15. Applicant: Lee-Meredith Industries, Inc.. Device class: 1.

Clearance details

Applicant: Lee-Meredith Industries, Inc.
Product code: Code IOL
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1989-12-28
Decision date: 1990-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOL

view all

K950376 — PARKER MODEL PM1995-09-06
K950377 — PARKER MODEL PE1995-09-06
K925839 — TRACKMASTER1993-06-24
K930261 — RTM REHABILITATION TREADMILL, MODEL #945-2001993-05-26
K904556 — MANSFIELD CARDIAC ASSIST MODEL 940(TM) IAB1991-12-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.