Meridian Co., Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K102375 | LUCIA | ILY | 2011-02-25 | View |
| 510(k) | K081962 | LAPEX BCS | ILY | 2008-12-29 | View |
| 510(k) | K034009 | LAPEX 2000 | NHN | 2005-01-21 | View |
| 510(k) | K023238 | MCPULSE | JOM | 2003-02-19 | View |
| 510(k) | K020360 | ABR-2000 | GZO | 2002-08-29 | View |
| 510(k) | K010897 | MERIDIAN-PORTABLE | GZO | 2001-06-19 | View |
| 510(k) | K001347 | MERIDIAN-II AND MERDIAN-PLUS | GZO | 2000-11-03 | View |
No matching devices.
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