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LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893217
510(k) Type
Traditional
Applicant
SHINHEN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1990
Days to Decision
258 days

LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893217
510(k) Type
Traditional
Applicant
SHINHEN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1990
Days to Decision
258 days