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MALE EXTERNAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K820565
510(k) Type
Traditional
Applicant
UROCARE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1982
Days to Decision
30 days

MALE EXTERNAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K820565
510(k) Type
Traditional
Applicant
UROCARE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1982
Days to Decision
30 days