# Electro Fiberoptics Corp.

- Location (FDA's records): Northborough, MA
- FDA decisions: 3 (1993–1994): 3 510(k) clearances
- Product codes: HRX (1), EQH (1), GCM (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
- K943628: Arthroscope (Nov 22, 1994)
- K933145: Fiberoptic Lightsources and Carriers (Sep 7, 1993)
- K921918: Fiber Optic Endoscope (Aug 17, 1993)

Source page: https://510kreport.com/company/electro-fiberoptics
