510(k) K890139— TOITU DOPPLER FETUS DETECTOR, FD-400D
Substantially EquivalentToitu of America, Inc.
Clearance details
- Applicant
- Toitu of America, Inc.
- Product code
- Code KNG
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wayne, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.