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NIM Standard Reinforced EMG Endotracheal Tube; CONTACT Reinforced EMG Endotracheal Tube

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230320
510(k) Type
Special
Applicant
Medtronic Xomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2023
Days to Decision
262 days
Submission Type
Summary

NIM Standard Reinforced EMG Endotracheal Tube; CONTACT Reinforced EMG Endotracheal Tube

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230320
510(k) Type
Special
Applicant
Medtronic Xomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2023
Days to Decision
262 days
Submission Type
Summary