DIAL-AWAY PAIN— 510(k) K904457

Substantially Equivalent

R.F.P., Inc.

FDA 510(k) clearance K904457 for DIAL-AWAY PAIN, Substantially Equivalent on 1991-04-03. Applicant: R.F.P., Inc.. Device class: 2.

Clearance details

Applicant: R.F.P., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1990-10-01
Decision date: 1991-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aurora, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZJ

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

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