NT MEDITENS PLUS, TYPE 290— 510(k) K014020

Name: FDA 510(k) clearance K014020
Creator: U.S. Food and Drug Administration
Published: 2002-07-11

Substantially Equivalent

Bio-Medical Research, Ltd.

FDA 510(k) clearance K014020 for NT MEDITENS PLUS, TYPE 290, Substantially Equivalent on 2002-07-11. Applicant: Bio-Medical Research, Ltd.. Device class: 2.

Clearance details

Applicant: Bio-Medical Research, Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2001-12-06
Decision date: 2002-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galway, IE

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZJ

view all

K252712 — STIMPOD NMS460 Nerve Stimulator2026-05-28
K252767 — actiTENS mini2026-01-16
K252236 — CP Relief Wand Rx - TENS/NMES2025-08-15
K232441 — Unipro (K-UNIPRO-US)2024-08-30
K241228 — TENSWave2024-08-27

More clearances from Bio-Medical Research, Ltd.

view all

K203513 — SLENDERTONE Evolve Abs, Type 7352021-02-10
DEN170049 — Innovo2018-11-06
K180688 — SLENDERTONE CoreFit Abs 8, Type 7342018-10-25
K161974 — SLENDERTONE® Connect Abs, Type 5702016-11-01
K151903 — Slendertone connect Abs2015-11-06

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