Radiotherapeutics Corp.
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE (K011220) | Radiotherapeutics Corp. | 2002-07-01 |
| LEVEEN ELECTRODE (K012315) | Radiotherapeutics Corp. | 2001-10-11 |
| RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR (K000241) | Radiotherapeutics Corp. | 2000-04-14 |
| LEVEEN NEEDLE ELECTRODE (K982556) | Radiotherapeutics Corp. | 2000-04-06 |
| LEVEEN NEEDLE ELECTRODE (K000032) | Radiotherapeutics Corp. | 2000-03-30 |
| MR COMPATIBLE LEVEEN NEEDLE ELECTRODE (K982854) | Radiotherapeutics Corp. | 1998-11-10 |
| RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR (K981672) | Radiotherapeutics Corp. | 1998-07-17 |
| RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000 (K972441) | Radiotherapeutics Corp. | 1997-09-04 |
| MODIFIED LEVEEN NEEDLE ELECTRODE (K962313) | Radiotherapeutics Corp. | 1996-09-11 |
| SENSOR SHEATH TS1 (K962386) | Radiotherapeutics Corp. | 1996-08-20 |
| RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 (K955144) | Radiotherapeutics Corp. | 1996-04-07 |
| LEVEEN NEEDLE ELECTRODE(TM) (K950347) | Radiotherapeutics Corp. | 1995-02-23 |
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Every clearance here is in the API, with alerts when new ones post.