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PULMOCATH INTRABRONCHIAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K901615
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1992
Days to Decision
966 days

PULMOCATH INTRABRONCHIAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K901615
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1992
Days to Decision
966 days