FDA product code EFC: Warmer, Anesthetic Tube
EFC is the FDA product code for warmer, anesthetic tube. It is a Class I device, regulated under 21 CFR 872.6100 and reviewed by the Dental panel. Devices under EFC reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Warmer, Anesthetic Tube |
| Device class | Class I |
| Regulation | 21 CFR 872.6100 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | 510(k) exempt |
Recalls for EFC devices
openFDA lists no recalls for product code EFC.
Frequently asked questions
What is FDA product code EFC?
EFC is the FDA product code for warmer, anesthetic tube. It is a Class I device, regulated under 21 CFR 872.6100 and reviewed by the Dental panel.
What device class is EFC?
Class I, regulation 21 CFR 872.6100. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code EFC
- Run a recall and safety report across every EFC manufacturer
- Watch product code EFC 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.