London Intl., LLC
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K982924 | DUREX SENSIDOM LATEX CONDOM | HIS | 1998-11-16 | View |
| 510(k) | K983380 | DUREX LUBRAGEL LATEX CONDOM | HIS | 1998-11-16 | View |
| 510(k) | K980174 | DUREX COLORS AND SCENTS | HIS | 1998-08-13 | View |
| 510(k) | K980785 | STERILE, POWDERFREE LATEX EXAMINATION GLOVE | LYY | 1998-06-10 | View |
| 510(k) | K980319 | DUREX ULTRA COMFORT | HIS | 1998-05-20 | View |
| 510(k) | K980204 | DUREX LATEX CONDOMS | HIS | 1998-04-17 | View |
No matching devices.
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