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PREGNANCY TEST KIT, OVER-THE-COUNTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780321
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1978
Days to Decision
39 days

PREGNANCY TEST KIT, OVER-THE-COUNTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780321
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1978
Days to Decision
39 days