CEFAR DUAL— 510(k) K883236

Substantially Equivalent

Cefar Medical Products, Inc.

FDA 510(k) clearance K883236 for CEFAR DUAL, Substantially Equivalent on 1988-11-16. Applicant: Cefar Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Cefar Medical Products, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-08-01
Decision date: 1988-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marlboro, NJ, 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.