RTM REHABILITATION TREADMILL, MODEL #945-200— 510(k) K930261

Name: FDA 510(k) clearance K930261
Creator: U.S. Food and Drug Administration
Published: 1993-05-26

Substantially Equivalent

Biodan Medical Systems, Ltd.

FDA 510(k) clearance K930261 for RTM REHABILITATION TREADMILL, MODEL #945-200, Substantially Equivalent on 1993-05-26. Applicant: Biodan Medical Systems, Ltd.. Device class: 1.

Clearance details

Applicant: Biodan Medical Systems, Ltd.
Product code: Code IOL
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1993-01-19
Decision date: 1993-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shirley, NY, 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
K904556 — MANSFIELD CARDIAC ASSIST MODEL 940(TM) IAB1991-12-18
K913518 — TA620 TREADMILL CONTROLLER1991-10-24

More clearances from Biodan Medical Systems, Ltd.

view all

K932153 — THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME1993-09-07
K930262 — TREATMENT TABLE, MODEL #825-1001993-03-29
K930259 — TRACTION TABLE MODEL #825-2001993-03-24
K926083 — NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPES1993-02-12
K926082 — CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT1992-12-30

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