Last synced on 22 September 2023 at 11:04 pm

KOTEX MAXI PADS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850033
510(k) Type
Traditional
Applicant
KIMBERLY-CLARK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1985
Days to Decision
57 days

KOTEX MAXI PADS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850033
510(k) Type
Traditional
Applicant
KIMBERLY-CLARK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1985
Days to Decision
57 days