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TROCAR CATHETER/THORACIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K792202
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1979
Days to Decision
18 days

TROCAR CATHETER/THORACIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K792202
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1979
Days to Decision
18 days