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CATHETER, NATURAL LATEX URETHRAL

Page Type
Cleared 510(K)
510(k) Number
K760440
510(k) Type
Traditional
Applicant
AKRON CATHETER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1976
Days to Decision
65 days

CATHETER, NATURAL LATEX URETHRAL

Page Type
Cleared 510(K)
510(k) Number
K760440
510(k) Type
Traditional
Applicant
AKRON CATHETER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1976
Days to Decision
65 days