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RUBBER CONTRACEPTIVE, LATEX CONDOMS

Page Type
Cleared 510(K)
510(k) Number
K875111
510(k) Type
Traditional
Applicant
OKAMOTO U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1988
Days to Decision
74 days

RUBBER CONTRACEPTIVE, LATEX CONDOMS

Page Type
Cleared 510(K)
510(k) Number
K875111
510(k) Type
Traditional
Applicant
OKAMOTO U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1988
Days to Decision
74 days