Last synced on 14 November 2025 at 11:06 pm

COVER-ALL MALE INCONTINENCE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K801629
510(k) Type
Traditional
Applicant
THE UROLOGY GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1980
Days to Decision
28 days

COVER-ALL MALE INCONTINENCE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K801629
510(k) Type
Traditional
Applicant
THE UROLOGY GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1980
Days to Decision
28 days