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CONTACT EMG ROTATABLE ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
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)
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