FDA product code EGQ: Injector, Jet, Gas-Powered
EGQ is the FDA product code for injector, jet, gas-powered. It is a Class II device, regulated under 21 CFR 872.4465 and reviewed by the Dental panel. FDA has cleared 1 510(k) submission under EGQ. The average 510(k) review took 200 days (median 200).
Classification
| Field | Value |
|---|---|
| Device name | Injector, Jet, Gas-Powered |
| Device class | Class II |
| Regulation | 21 CFR 872.4465 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Compare with all 510(k) review times · Search every EGQ clearance
Top EGQ applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Wilson-Cook Medical, Inc. | 1 | 1990-10-09 |
Most recent EGQ clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K901348 | Wilson-Cook Medical, Inc. | WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS | 1990-10-09 | 200 |
Recalls for EGQ devices
openFDA lists no recalls for product code EGQ.
Frequently asked questions
What is FDA product code EGQ?
EGQ is the FDA product code for injector, jet, gas-powered. It is a Class II device, regulated under 21 CFR 872.4465 and reviewed by the Dental panel.
What device class is EGQ?
Class II, regulation 21 CFR 872.4465. Typical premarket route: 510(k).
How long does a 510(k) take for product code EGQ?
Across 1 cleared submissions the average was 200 days from receipt to decision (median 200).
Which companies have the most EGQ clearances?
Wilson-Cook Medical, Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code EGQ
- Run a recall and safety report across every EGQ manufacturer
- Watch product code EGQ for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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