FDA product code OGB: Caudal Anesthesia Kit
OGB is the FDA product code for caudal anesthesia kit. It is a Class II device, regulated under 21 CFR 868.5140 and reviewed by the Anesthesiology panel. Devices under OGB 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 | Caudal Anesthesia Kit |
| Device class | Class II |
| Regulation | 21 CFR 868.5140 |
| Review panel | AN — Anesthesiology |
| Medical specialty | Anesthesiology |
| Premarket route | 510(k) exempt |
Recalls for OGB devices
openFDA lists no recalls for product code OGB.
Frequently asked questions
What is FDA product code OGB?
OGB is the FDA product code for caudal anesthesia kit. It is a Class II device, regulated under 21 CFR 868.5140 and reviewed by the Anesthesiology panel.
What device class is OGB?
Class II, regulation 21 CFR 868.5140. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code OGB
- Run a recall and safety report across every OGB manufacturer
- Watch product code OGB 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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