NAIMCO, INC., IONTOPHORESIS DRUG DELIVERY ELECTRODES, MODELS 201-400, 201-401, 201-402, 201-403 AND 201-405— 510(k) K040495

Name: FDA 510(k) clearance K040495
Creator: U.S. Food and Drug Administration
Published: 2004-04-22

Substantially Equivalent

Naimco, Inc.

FDA 510(k) clearance K040495 for NAIMCO, INC., IONTOPHORESIS DRUG DELIVERY ELECTRODES, MODELS 201-400, 201-401, 201-402, 201-403 AND 201-405, Substantially Equivalent on 2004-04-22. Applicant: Naimco, Inc.. Device class: 2.

Clearance details

Applicant: Naimco, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2004-02-26
Decision date: 2004-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chattanooga, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EGJ

view all

K242041 — STOPWET iontophoresis apparatus (SW01)2025-04-01
K241267 — Hidroxa SE302024-10-17
K232020 — Iontophoresis Electrodes2023-10-16
K192749 — Dermadry2020-02-10
K191436 — Saalio2019-10-18

More clearances from Naimco, Inc.

view all

K063135 — SONIC-STIM2007-02-05
K050469 — EZ-STIK ELECTRODES2005-05-13

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