# Renovorx, Inc.

- Location (FDA's records): Los Altos, CA
- FDA decisions: 4 (2014–2021): 4 510(k) clearances
- Product codes: MJN (4)
- 510(k) review time since 2016: median 51 days, against 116 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Thermopeutix, Inc.: 1 (https://510kreport.com/company/thermopeutix)

## Its most-cited devices
- K191606: RenovoCath (2019), cited by 1
- K160067: RenovoCath (2017), cited by 1

## Recent decisions
- K212324: RenovoCath (Aug 23, 2021)
- K191606: RenovoCath (Aug 7, 2019)
- K160067: RenovoCath (Mar 7, 2017)
- K141175: Renovocath RC120 (Oct 24, 2014)

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