Toitu of America, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Toitu of America, Inc. makes
Toitu of America, Inc. manufactures fetal monitoring equipment, including the FD-400D Doppler fetus detector and the MT-332 fetal actocardiograph.
The company is based in the United States, and its portfolio consists of Class II medical devices that are listed in the FDA 510(k) regulatory registry.
Catalogue
Toitu Doppler Fetus Detector, Fd-400D Ref K890139
Regimes: 510(k) Registry: 510(k)Toitu Fetal Actocardiograph, Mt-332 Ref K894036
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Toitu of America, Inc. have in the registry?
The registry currently lists 2 devices for Toitu of America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Toitu of America, Inc.'s devices?
Among its 2 most recently registered devices, Toitu of America, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Toitu of America, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Toitu of America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Toitu of America, Inc. in the registry?
The most recently registered devices listed for Toitu of America, Inc. include TOITU DOPPLER FETUS DETECTOR, FD-400D and TOITU FETAL ACTOCARDIOGRAPH, MT-332.