Last synced on 27 January 2023 at 11:04 pm

Allergan Botox Needle Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173815
510(k) Type
Traditional
Applicant
Natus Manufacturing Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
6/29/2018
Days to Decision
196 days
Submission Type
Summary

Allergan Botox Needle Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173815
510(k) Type
Traditional
Applicant
Natus Manufacturing Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
6/29/2018
Days to Decision
196 days
Submission Type
Summary