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CATHETER, AKRON FOLEY TEFLON

Page Type
Cleared 510(K)
510(k) Number
K781751
510(k) Type
Traditional
Applicant
LATEX IND., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1979
Days to Decision
98 days

CATHETER, AKRON FOLEY TEFLON

Page Type
Cleared 510(K)
510(k) Number
K781751
510(k) Type
Traditional
Applicant
LATEX IND., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1979
Days to Decision
98 days