London International Group, Inc.
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) | K991677 | REGENT SKINDENDE EXAM GLOVE, REGENT BIOGEL D, REGENTBIOGEL DIAGNOSTIC (POWDERFREE) | LYY | 2000-04-12 | View |
| 510(k) | K984249 | SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE | LZA | 1999-05-04 | View |
| 510(k) | K980942 | REGENT BIOGEL INDICATOR INNER SURGICAL GLOVE | KGO | 1998-05-11 | View |
| 510(k) | K980516 | REGENT BIOGEL ORTHOPEDIC SURGICAL GLOVE | KGO | 1998-04-23 | View |
| 510(k) | K971514 | REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE | LYY | 1997-10-29 | View |
No matching devices.
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