EMG RECORDING ELECTRODE ASSEMBLY— 510(k) K120342

Substantially Equivalent

Rhythmlink International, LLC

FDA 510(k) clearance K120342 for EMG RECORDING ELECTRODE ASSEMBLY, Substantially Equivalent on 2012-06-22. Applicant: Rhythmlink International, LLC.

Clearance details

Applicant
Rhythmlink International, LLC
Product code
Code IKT
Advisory panel
Physical Medicine
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Columbia, SC, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.