Suzhou Colour-Way Enterprise Development Co., Ltd.
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) | K121925 | POWDERED LATEX SURGEON'S GLOVE | KGO | 2013-08-28 | View |
| 510(k) | K083817 | M. DIOR BRAND | HIS | 2009-09-16 | View |
No matching devices.
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