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REMED MALE LATEX CONDOM (SUPER DUPER) PREVENTOR, LUCKY BOY, AND SUMMIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993390
510(k) Type
Abbreviated
Applicant
REMED PHARMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2000
Days to Decision
129 days
Submission Type
Statement

REMED MALE LATEX CONDOM (SUPER DUPER) PREVENTOR, LUCKY BOY, AND SUMMIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993390
510(k) Type
Abbreviated
Applicant
REMED PHARMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2000
Days to Decision
129 days
Submission Type
Statement