D.B.I. America Corp.
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) | K051910 | MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER | ELC | 2005-09-02 | View |
| 510(k) | K981990 | MRS-400, MAXI 400, MRSL-400, MAXI 400L | EFB | 1998-06-22 | View |
No matching devices.
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