# Peter M. Rothenberg, M.D.

- Location (FDA's records): San Clemente, CA
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: LDF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Romedex International Srl: 1 (https://510kreport.com/company/romedex-international)
- Remington Medical, Inc.: 1 (https://510kreport.com/company/remington-medical)

## Its most-cited devices
- K032613: Temporary Transvenous Pacemaker Placement Assist Device (2003), cited by 2

## Recent decisions
- K032613: Temporary Transvenous Pacemaker Placement Assist Device (Nov 20, 2003)

Source page: https://510kreport.com/company/peter-m-rothenberg-md