Toitu of America, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K894036 | TOITU FETAL ACTOCARDIOGRAPH, MT-332 | HGM | 1989-11-06 | View |
| 510(k) | K890139 | TOITU DOPPLER FETUS DETECTOR, FD-400D | KNG | 1989-03-29 | View |
No matching devices.
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