DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND PRIVATE LABELED— 510(k) K062437

Substantially Equivalent

Technomed Europe

FDA 510(k) clearance K062437 for DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND PRIVATE LABELED, Substantially Equivalent on 2007-02-16. Applicant: Technomed Europe. Device class: 2.

Clearance details

Applicant
Technomed Europe
Product code
Code IKT
Device class
Class 2
Regulation
21 CFR 890.1385
Advisory panel
Physical Medicine
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Maastricht-Airport, NL
Download summary PDFView on FDA.gov ↗

Recent devices under product code IKT

view all

More clearances from Technomed Europe

view all

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