# Applied Fiberoptics, Inc.

- Location (FDA's records): Southbridge, MA
- FDA decisions: 3 (1982–1997): 3 510(k) clearances
- Product codes: FGB (1), EQH (1), FAJ (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
- K964037: Flexible Cystoscope (Feb 20, 1997)
- K964482: Flexible Ureteroscope (Jan 24, 1997)
- K820621: Nasal Instruments (Mar 19, 1982)

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