TOITU DOPPLER FETUS DETECTOR, FD-400D— 510(k) K890139
Substantially EquivalentToitu of America, Inc.
FDA 510(k) clearance K890139 for TOITU DOPPLER FETUS DETECTOR, FD-400D, Substantially Equivalent on 1989-03-29. Applicant: Toitu of America, Inc.. Device class: 2.
Clearance details
- Applicant
- Toitu of America, Inc.
- Product code
- Code KNG
- Device class
- Class 2
- Regulation
- 21 CFR 884.2660
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wayne, PA, US
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