Innolatex Sdn. Bhd
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K053367 | MALE NATURAL RUBBER LATEX CONDOM | HIS | 2006-02-21 | View |
| 510(k) | K041837 | INNOLATEX MALE LATEX CONDOMS COLORED AND SCENTED | HIS | 2004-09-24 | View |
| 510(k) | K012664 | ULTRA THICK MALE LATEX CONDOM WITH SILICONE LUBRICANT | HIS | 2001-11-09 | View |
| 510(k) | K012964 | 56MM CONDOM,MALE NATURAL RUBBER LATEX CONDOM | HIS | 2001-11-09 | View |
| 510(k) | K012962 | DOTTED CONDOM, MALE NATURAL RUBBER LATEX CONDOM | HIS | 2001-11-09 | View |
| 510(k) | K012665 | ULTRA THIN MALE LATEX CONDOM WITH SILICONE LUBRICANT | HIS | 2001-11-09 | View |
| 510(k) | K010919 | MALE NATURAL RUBBER LATEX CONDOM | HIS | 2001-06-15 | View |
| 510(k) | K010178 | SPERMICIDAL LUBRICATED MALE LATEX CONDOM | LTZ | 2001-04-27 | View |
| 510(k) | K002393 | NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM | HIS | 2000-12-19 | View |
No matching devices.
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