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GENUA MENOPAUSE MONITOR TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002450
510(k) Type
Traditional
Applicant
GENUA 1944, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2001
Days to Decision
156 days
Submission Type
Statement

GENUA MENOPAUSE MONITOR TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002450
510(k) Type
Traditional
Applicant
GENUA 1944, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2001
Days to Decision
156 days
Submission Type
Statement