Last synced on 14 November 2025 at 11:06 pm

PATIENT UNDERPAD

Page Type
Cleared 510(K)
510(k) Number
K813263
510(k) Type
Traditional
Applicant
THE BUCKEYE CELLULOSE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1981
Days to Decision
7 days

PATIENT UNDERPAD

Page Type
Cleared 510(K)
510(k) Number
K813263
510(k) Type
Traditional
Applicant
THE BUCKEYE CELLULOSE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1981
Days to Decision
7 days