Last synced on 23 September 2022 at 11:05 pm

COOPDECH ENDOBRONCHIAL BLOCKER TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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