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CONTACT EMG ROTATABLE ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050162
510(k) Type
Traditional
Applicant
MEDTRONIC XOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2005
Days to Decision
37 days
Submission Type
Summary

CONTACT EMG ROTATABLE ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050162
510(k) Type
Traditional
Applicant
MEDTRONIC XOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2005
Days to Decision
37 days
Submission Type
Summary