RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R— 510(k) K982967

Name: FDA 510(k) clearance K982967
Creator: U.S. Food and Drug Administration
Published: 1999-02-23

Substantially Equivalent

Woodside Biomedical, Inc.

FDA 510(k) clearance K982967 for RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R, Substantially Equivalent on 1999-02-23. Applicant: Woodside Biomedical, Inc.. Device class: 2.

Clearance details

Applicant: Woodside Biomedical, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1998-08-25
Decision date: 1999-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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 Woodside Biomedical, Inc.

view all

K020180 — RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL2002-03-21
K994387 — RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL2000-03-16
K983907 — RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R1999-12-09
K982436 — RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R1998-10-08
K980333 — RELIEFBAND1998-02-18

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