ELECTRODE NEEDLES— 510(k) K990015
Substantially EquivalentTechnomed Europe
FDA 510(k) clearance K990015 for ELECTRODE NEEDLES, Substantially Equivalent on 1999-05-27. 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
- 6191 Bg Beek, NL
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