Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Boston ScientificLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Radiotherapeutics Corporation with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 1, 2002: LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE.
| Jul 1, 2002 | LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODEK011220 · GEI | 510(k) clearances |
| Oct 11, 2001 | LEVEEN ELECTRODEK012315 · GEI | 510(k) clearances |
| Apr 14, 2000 | RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATORK000241 · GEI | 510(k) clearances |
| Apr 6, 2000 | LEVEEN NEEDLE ELECTRODEK982556 · GEI | 510(k) clearances |
| Mar 30, 2000 | LEVEEN NEEDLE ELECTRODEK000032 · GEI | 510(k) clearances |
| Nov 10, 1998 | MR COMPATIBLE LEVEEN NEEDLE ELECTRODEK982854 · GEI | 510(k) clearances |
| Jul 17, 1998 | RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATORK981672 · GEI | 510(k) clearances |
| Sep 4, 1997 | RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000K972441 · GEI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
