DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE— 510(k) K001869
Substantially EquivalentMedicotest A/S
FDA 510(k) clearance K001869 for DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE, Substantially Equivalent on 2000-09-18. 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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