Kerr Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K091613 | TAKE 1 | ELW | 2009-10-07 | View |
| 510(k) | K090292 | PREMISE MODIFIED | EBF | 2009-04-03 | View |
| 510(k) | K081695 | DMC COMPOSITE | EBF | 2008-08-12 | View |
| 510(k) | K072622 | STANDOUT 2 | ELW | 2007-12-04 | View |
| 510(k) | K042888 | DEMETRON IDS CURING LIGHT | EBZ | 2004-11-10 | View |
| 510(k) | K031484 | STAND OUT | ELW | 2003-07-03 | View |
| 510(k) | K014179 | DEMETRON LC | EBZ | 2002-02-04 | View |
| 510(k) | K010994 | TAKE ONE BITE MODIFIED | ELW | 2001-04-23 | View |
| 510(k) | K001655 | PERMLASTIC 2 | ELW | 2000-08-10 | View |
No matching devices.
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