Teknomed, Inc.
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) | K925395 | TECHNOMED PULSOLITH 4000 LASER SYSTEM | LNK | 1993-05-21 | View |
| 510(k) | K920708 | MULTILASE 2500 A | GEX | 1992-11-05 | View |
| 510(k) | K913917 | MULTILASE 2100 C, 2100 D | GEX | 1992-11-05 | View |
| 510(k) | K913290 | MULTILASE 2100 A | GEX | 1992-02-21 | View |
| 510(k) | K895178 | TECHNOMED PULSOLITH LASER SYSTEM | FFK | 1989-10-06 | View |
| 510(k) | K890436 | TECHNOMED PULSOLITH LASER SYSTEM | FFK | 1989-03-23 | View |
| 510(k) | K790132 | TECNOTOMO | IZF | 1979-02-21 | View |
No matching devices.
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