K-number	K161430
Device name	Myoject Luer Lock Needle Electrode
Applicant	Natus Manufacturing Limited
Product code	IKT
Device class	Class II
Decision date	Mar 2, 2017
Decision	Substantially Equivalent
Regulation	890.1385

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Source

View the full FDA submission: accessdata.fda.gov

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Myoject Luer Lock Needle Electrode

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