Puricore, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K123072 | VASHE WOUND THERAPY SOLUTION | FRO | 2013-02-14 | View |
| 510(k) | K123071 | VASHE SKIN AND WOUND HYDROGEL | FRO | 2013-01-24 | View |
| 510(k) | K100918 | VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014 | FRO | 2010-08-09 | View |
| 510(k) | K093697 | VASHE WOUND THERAPY SOLUTION | FRO | 2010-04-13 | View |
| 510(k) | K093155 | VASHE WOUND CLEANSING SYSTEM | FRO | 2010-03-01 | View |
| 510(k) | K092232 | MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014 | FRO | 2009-08-19 | View |
| 510(k) | K063159 | STERILOX LIQUID CHEMICAL STERILANT SYSTEM | MED | 2007-04-02 | View |
| 510(k) | K061689 | AQUATINE EC ENDODONTIC CLEANSER | KJJ | 2006-08-24 | View |
No matching devices.
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