Radiotherapeutics Corp.
FDA 510(k) & PMA Approved Devices — 12 products
Advertisement
Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K011220 | LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE | GEI | 2002-07-01 | View |
| 510(k) | K012315 | LEVEEN ELECTRODE | GEI | 2001-10-11 | View |
| 510(k) | K000241 | RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR | GEI | 2000-04-14 | View |
| 510(k) | K982556 | LEVEEN NEEDLE ELECTRODE | GEI | 2000-04-06 | View |
| 510(k) | K000032 | LEVEEN NEEDLE ELECTRODE | GEI | 2000-03-30 | View |
| 510(k) | K982854 | MR COMPATIBLE LEVEEN NEEDLE ELECTRODE | GEI | 1998-11-10 | View |
| 510(k) | K981672 | RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR | GEI | 1998-07-17 | View |
| 510(k) | K972441 | RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000 | GEI | 1997-09-04 | View |
| 510(k) | K962313 | MODIFIED LEVEEN NEEDLE ELECTRODE | JOS | 1996-09-11 | View |
| 510(k) | K962386 | SENSOR SHEATH TS1 | FLL | 1996-08-20 | View |
| 510(k) | K955144 | RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 | GEI | 1996-04-07 | View |
| 510(k) | K950347 | LEVEEN NEEDLE ELECTRODE(TM) | GEI | 1995-02-23 | View |
No matching devices.
Advertisement