# Radiotherapeutics Corp.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 12 (1995–2002): 12 510(k) clearances
- Product codes: GEI (10), JOS (1), FLL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 12 (0 its own)
- Recalls linked to its devices: 15 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Boston Scientific Corp: 3 (https://510kreport.com/company/boston-scientific)
- Stellartech Research Corp.: 3 (https://510kreport.com/company/stellartech-research)
- Vivant Medical, Inc.: 2 (https://510kreport.com/company/vivant-medical)
- Valleylab, Inc.: 2 (https://510kreport.com/company/valleylab)
- Neuwave Medical, Inc.: 1 (https://510kreport.com/company/neuwave-medical)
- Barrx Medical, Incorporated: 1 (https://510kreport.com/company/barrx-medical)

## Its most-cited devices
- K981672: Radiotherapeutics RF-2000 Radiofrequency Generator (1998), cited by 4
- K000241: Radiotherapeutics RF 3000 Radiofrequency Generator (2000), cited by 3
- K012315: Leveen Electrode (2001), cited by 2
- K962313: Modified Leveen Needle Electrode (1996), cited by 1
- K982556: Leveen Needle Electrode (2000), cited by 1
- K000032: Leveen Needle Electrode (2000), cited by 1

## Recent decisions
- K011220: Leveen Reflect Monopolar/Bipolar Needle Electrode (Jul 1, 2002)
- K012315: Leveen Electrode (Oct 11, 2001)
- K000241: Radiotherapeutics RF 3000 Radiofrequency Generator (Apr 14, 2000)
- K982556: Leveen Needle Electrode (Apr 6, 2000)
- K000032: Leveen Needle Electrode (Mar 30, 2000)
- K982854: MR Compatible Leveen Needle Electrode (Nov 10, 1998)
- K981672: Radiotherapeutics RF-2000 Radiofrequency Generator (Jul 17, 1998)
- K972441: Radiotherapeutics RF Generator. Model #RF-2000 (Sep 4, 1997)

Source page: https://510kreport.com/company/radiotherapeutics