# Robert Bosch Corp.

- Location (FDA's records): St. James, NY
- FDA decisions: 21 (1979–1986): 21 510(k) clearances
- Product codes: ESD (5), DRT (4), IPF (3), IMJ (1), IMI (1), LDD (1), ISB (1), ISA (1), ETW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K854493: Erg 555 Couch Ergometer (Jun 16, 1986)
- K854491: Erg 550 Ergometer Bicycle (Jun 16, 1986)
- K854492: Erg 551 Ergometer, Bicycle (Jun 16, 1986)
- K853154: HV-4 (Mar 28, 1986)
- K853541: SP 4 (Mar 28, 1986)
- K853271: Hearing Aid Analysis System (Jan 16, 1986)
- K851485: DEFI 502 (Aug 29, 1985)
- K840717: ECS 502 (Aug 19, 1985)

Source page: https://510kreport.com/company/robert-bosch