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KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113333
510(k) Type
Traditional
Applicant
KIMBERLY-CLARK CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2012
Days to Decision
179 days
Submission Type
Summary

KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113333
510(k) Type
Traditional
Applicant
KIMBERLY-CLARK CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2012
Days to Decision
179 days
Submission Type
Summary