EMG RECORDING ELECTRODE ASSEMBLY— 510(k) K120342
Substantially EquivalentRhythmlink International, LLC
FDA 510(k) clearance K120342 for EMG RECORDING ELECTRODE ASSEMBLY, Substantially Equivalent on 2012-06-22. Applicant: Rhythmlink International, LLC. Device class: 2.
Clearance details
- Applicant
- Rhythmlink International, LLC
- 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
- Columbia, SC, US
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