CYCLOTEC AMT CTI TENS DEVICE— 510(k) K010615

Substantially Equivalent

Cyclotec

FDA 510(k) clearance K010615 for CYCLOTEC AMT CTI TENS DEVICE, Substantially Equivalent on 2001-10-12. Applicant: Cyclotec. Device class: 2.

Clearance details

Applicant: Cyclotec
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2001-03-01
Decision date: 2001-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lauderhill, FL, 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.