DISPOSABLE NEEDLE ELECTRODE— 510(k) K961013
Substantially EquivalentMedelec Intl. Corp.
FDA 510(k) clearance K961013 for DISPOSABLE NEEDLE ELECTRODE, Substantially Equivalent on 1996-12-20. Applicant: Medelec Intl. Corp.. Device class: 2.
Clearance details
- Applicant
- Medelec Intl. Corp.
- 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
- England, GB
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