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OVUSIGN - ONE-STEP HOME OVULATION PREDICTOR TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963693
510(k) Type
Traditional
Applicant
PRINCETON BIOMEDITECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1996
Days to Decision
74 days
Submission Type
Statement

OVUSIGN - ONE-STEP HOME OVULATION PREDICTOR TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963693
510(k) Type
Traditional
Applicant
PRINCETON BIOMEDITECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1996
Days to Decision
74 days
Submission Type
Statement