Midwest Dental Products Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K973800 | 23:1 REDUCTION ANGLE | EGS | 1998-03-11 | View |
| 510(k) | K964755 | MICROJET CAVITY PREPARATION SYSTEM | KOJ | 1997-09-11 | View |
| 510(k) | K962877 | MIDWEST 300 SE | EFB | 1996-10-18 | View |
| 510(k) | K963050 | TRADITION P, PUSH BUTTON HANDPIECE | EFB | 1996-10-11 | View |
| 510(k) | K955655 | MIDWEST ONE | EFB | 1996-03-05 | View |
No matching devices.
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