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OVUTIME OVULATION PREDICTOR TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853142
510(k) Type
Traditional
Applicant
ADVANCED CARE PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1985
Days to Decision
141 days

OVUTIME OVULATION PREDICTOR TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853142
510(k) Type
Traditional
Applicant
ADVANCED CARE PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1985
Days to Decision
141 days