# Virtual Corp.

- Location (FDA's records): Portland, OR
- FDA decisions: 9 (1985–1996): 9 510(k) clearances
- Product codes: EWO (3), EWD (2), ETY (2), GWJ (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
- K960500: The Virtual M-332 (Apr 3, 1996)
- K934715: Model 222 Clinical Audiometer (May 10, 1994)
- K930203: Model 322 Clinical Audiometer (Jul 8, 1993)
- K926574: Model 330 Screening Audio Meter, Modified (Mar 29, 1993)
- K911689: Model 330 Screening Audiometer (Oct 21, 1991)
- K896301: Model 340 Probe Mic System (Jan 16, 1990)
- K895443: Model 210 Impedance System (Jan 16, 1990)
- K863984: Model 320 Two Channel Audiometer (Nov 18, 1986)

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