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MODIFIED ENDOBRONCHIAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902116
510(k) Type
Traditional
Applicant
CONCORD/PORTEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1990
Days to Decision
85 days

MODIFIED ENDOBRONCHIAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902116
510(k) Type
Traditional
Applicant
CONCORD/PORTEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1990
Days to Decision
85 days