FDA product code OGC: Continuous Brachial Plexus Block Tray
OGC is the FDA product code for continuous brachial plexus block tray. It is a Class II device, regulated under 21 CFR 868.5150 and reviewed by the Anesthesiology panel. Devices under OGC reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
Classification
| Field | Value |
|---|---|
| Device name | Continuous Brachial Plexus Block Tray |
| Device class | Class II |
| Regulation | 21 CFR 868.5150 |
| Review panel | AN — Anesthesiology |
| Medical specialty | Anesthesiology |
| Premarket route | 510(k) exempt |
Recalls for OGC devices
openFDA lists no recalls for product code OGC.
Frequently asked questions
What is FDA product code OGC?
OGC is the FDA product code for continuous brachial plexus block tray. It is a Class II device, regulated under 21 CFR 868.5150 and reviewed by the Anesthesiology panel.
What device class is OGC?
Class II, regulation 21 CFR 868.5150. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code OGC
- Run a recall and safety report across every OGC manufacturer
- Watch product code OGC 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.