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TOITU DOPPLER FETUS DETECTOR, FD-400D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890139
510(k) Type
Traditional
Applicant
TOITU OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1989
Days to Decision
75 days

TOITU DOPPLER FETUS DETECTOR, FD-400D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890139
510(k) Type
Traditional
Applicant
TOITU OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1989
Days to Decision
75 days