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