MULTI-STIM, MODEL MS-100— 510(k) K001897

Name: FDA 510(k) clearance K001897
Creator: U.S. Food and Drug Administration
Published: 2001-06-12

Substantially Equivalent

Metron Medical Australia, Pty, Ltd.

FDA 510(k) clearance K001897 for MULTI-STIM, MODEL MS-100, Substantially Equivalent on 2001-06-12. Applicant: Metron Medical Australia, Pty, Ltd.. Device class: 2.

Clearance details

Applicant: Metron Medical Australia, Pty, Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2000-06-21
Decision date: 2001-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carrum Downs, AU

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 Metron Medical Australia, Pty, Ltd.

view all

K132137 — MULTISTIM2013-09-12
K124010 — ACCUSONIC ADVANTAGE2013-08-23
K120171 — ACCUSONIC ADVANTAGE2012-05-04
K030880 — VECTORSONIC, MODEL VU-2702003-04-18
K030648 — VECTORSURGE 5 MODEL 4702003-03-28

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