The following data is part of a premarket notification filed by Virtual Corp. with the FDA for Model 322 Clinical Audiometer.
| Device ID | K930203 |
| 510k Number | K930203 |
| Device Name: | MODEL 322 CLINICAL AUDIOMETER |
| Classification | Protector, Hearing (insert) |
| Applicant | VIRTUAL CORP. 521 SW 11TH SUITE 400 Portland, OR 97205 |
| Contact | Jonathan D Birck |
| Correspondent | Jonathan D Birck VIRTUAL CORP. 521 SW 11TH SUITE 400 Portland, OR 97205 |
| Product Code | EWD |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-14 |
| Decision Date | 1993-07-08 |