Last synced on 23 September 2022 at 11:05 pm

Myoject Luer Lock Needle Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161430
510(k) Type
Traditional
Applicant
Natus Manufacturing Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/2/2017
Days to Decision
283 days
Submission Type
Summary

Myoject Luer Lock Needle Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161430
510(k) Type
Traditional
Applicant
Natus Manufacturing Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/2/2017
Days to Decision
283 days
Submission Type
Summary