NEUROLINE, SUBDERMAL NEEDLE ELECTRODES— 510(k) K020907
Substantially EquivalentMedicotest A/S
FDA 510(k) clearance K020907 for NEUROLINE, SUBDERMAL NEEDLE ELECTRODES, Substantially Equivalent on 2002-06-14. Applicant: Medicotest A/S. Device class: 2.
Clearance details
- Applicant
- Medicotest A/S
- 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
- Washington, DC, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.