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DIAGNOSTIC DILATATION & MENSTRUAL KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840384
510(k) Type
Traditional
Applicant
INTL. MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1984
Days to Decision
91 days

DIAGNOSTIC DILATATION & MENSTRUAL KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840384
510(k) Type
Traditional
Applicant
INTL. MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1984
Days to Decision
91 days