Virtual Corp.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Virtual Corp.” (first 1985, latest 1996), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 92 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| EWO | Audiometer | 3 | 3 |
| ETY | Tester, Auditory Impedance | 2 | 2 |
| EWD | Protector, Hearing (Insert) | 2 | 2 |
| ETW | Calibrator, Hearing Aid / Earphone And Analysis Systems | 1 | 1 |
| GWJ | Stimulator, Auditory, Evoked Response | 1 | 1 |
Review panels
- Ear, Nose and Throat (8)
- Neurology (1)
Most recent Virtual Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K960500 | THE VIRTUAL M-332 | EWD | 1996-04-03 | 61 |
| K934715 | MODEL 222 CLINICAL AUDIOMETER | EWO | 1994-05-10 | 221 |
| K930203 | MODEL 322 CLINICAL AUDIOMETER | EWD | 1993-07-08 | 175 |
| K926574 | MODEL 330 SCREENING AUDIO METER, MODIFIED | GWJ | 1993-03-29 | 89 |
| K911689 | MODEL 330 SCREENING AUDIOMETER | EWO | 1991-10-21 | 188 |
| K896301 | MODEL 340 PROBE MIC SYSTEM | ETW | 1990-01-16 | 78 |
| K895443 | MODEL 210 IMPEDANCE SYSTEM | ETY | 1990-01-16 | 130 |
| K863984 | MODEL 320 TWO CHANNEL AUDIOMETER | EWO | 1986-11-18 | 35 |
| K853863 | MODEL 310 IMPEDANCE SYSTEM | ETY | 1985-12-18 | 92 |
Recalls
openFDA lists no recalls under a recalling firm named Virtual Corp..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Virtual Imaging, Inc. (9 510(k)s)
- Virtual Radiologic Corporation (3 510(k)s)
- Virtual Ports, Ltd. (2 510(k)s)
- Virtual Incision (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Virtual Corp.?
FDA lists 9 510(k) clearances under the applicant name “Virtual Corp.” (first 1985, latest 1996), across 5 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Virtual Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Virtual Corp. is 92 days.
Which FDA product codes appear under Virtual Corp.?
The most frequent FDA product codes under this applicant name are EWO (Audiometer, 3); ETY (Tester, Auditory Impedance, 2); EWD (Protector, Hearing (Insert), 2).
Next steps
- See all 9 Virtual Corp. clearances with predicates and recalls
- Run predicate analysis for product code EWO, Virtual Corp.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.