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CARDIO-ESOPHASCOPE

Page Type
Cleared 510(K)
510(k) Number
K830716
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1983
Days to Decision
157 days

CARDIO-ESOPHASCOPE

Page Type
Cleared 510(K)
510(k) Number
K830716
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1983
Days to Decision
157 days