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INTRAFLON, INTRAFLUX, INTRAVALVE

Page Type
Cleared 510(K)
510(k) Number
K813144
510(k) Type
Traditional
Applicant
EXCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1981
Days to Decision
22 days

INTRAFLON, INTRAFLUX, INTRAVALVE

Page Type
Cleared 510(K)
510(k) Number
K813144
510(k) Type
Traditional
Applicant
EXCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1981
Days to Decision
22 days