Shinemound Enterprise, 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) | K051913 | POWDERED LATEX PATIENT EXAMINATION GLOVES | LYY | 2005-09-30 | View |
| 510(k) | K994248 | SENSI-PRO, DISPOSABLE PRE-POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES | LYZ | 2000-01-28 | View |
| 510(k) | K994258 | SENSI-PRO DISPOSABLE POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES | LYZ | 2000-01-20 | View |
| 510(k) | K993240 | SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES | LYZ | 1999-10-27 | View |
| 510(k) | K993231 | SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES | LYZ | 1999-10-27 | View |
| 510(k) | K971360 | SYNTEX | LYZ | 1997-12-22 | View |
| 510(k) | K972104 | LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES | LYZ | 1997-08-15 | View |
| 510(k) | K970625 | POLY-MED | LYY | 1997-03-27 | View |
No matching devices.
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