Last synced on 19 July 2024 at 11:05 pm

ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080105
510(k) Type
Traditional
Applicant
CHILECOM MEDICAL DEVICES CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2009
Days to Decision
396 days
Submission Type
Summary

ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080105
510(k) Type
Traditional
Applicant
CHILECOM MEDICAL DEVICES CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2009
Days to Decision
396 days
Submission Type
Summary