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MODEL OB-500 FETAL GROWTH ANALYSIS & OPTION OBLINK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900271
510(k) Type
Traditional
Applicant
DIGISONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1990
Days to Decision
90 days

MODEL OB-500 FETAL GROWTH ANALYSIS & OPTION OBLINK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900271
510(k) Type
Traditional
Applicant
DIGISONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1990
Days to Decision
90 days