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REINFORCED SILICONE TRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K830352
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/1983
Days to Decision
33 days

REINFORCED SILICONE TRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K830352
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/1983
Days to Decision
33 days