Last synced on 14 November 2025 at 11:06 pm

MODIFIED ENDOBRONCHIAL TUBE

Page Type
Cleared 510(K)
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)
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