Last synced on 30 September 2022 at 11:05 pm

MODIFIED LABELING ON OKAMOTO HARMONY CONDOM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896339
510(k) Type
Traditional
Applicant
OKAMOTO U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1990
Days to Decision
68 days

MODIFIED LABELING ON OKAMOTO HARMONY CONDOM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896339
510(k) Type
Traditional
Applicant
OKAMOTO U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1990
Days to Decision
68 days