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COOPDECH ENDOBRONCHIAL BLOCKER TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093888
510(k) Type
Traditional
Applicant
Daiken Medical Co, Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/16/2010
Days to Decision
88 days
Submission Type
Summary

COOPDECH ENDOBRONCHIAL BLOCKER TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093888
510(k) Type
Traditional
Applicant
Daiken Medical Co, Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/16/2010
Days to Decision
88 days
Submission Type
Summary