FDA product code OGK: Orotracheal Intubation Guide Kit

OGK is the FDA product code for orotracheal intubation guide kit. It is a Class II device, regulated under 21 CFR 868.1400 and reviewed by the Anesthesiology panel. Devices under OGK reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. FDA has posted 2 recalls for OGK devices.

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 kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market.

Classification

Recalls for OGK devices

2 product recalls in 2 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2021-08-04.

Frequently asked questions

What is FDA product code OGK?

OGK is the FDA product code for orotracheal intubation guide kit. It is a Class II device, regulated under 21 CFR 868.1400 and reviewed by the Anesthesiology panel.

What device class is OGK?

Class II, regulation 21 CFR 868.1400. Typical premarket route: 510(k) exempt.

Have OGK devices been recalled?

Yes: 2 product recalls across 2 recall events; the most recent began 2021-08-04.

Next steps

• Run an FDA pathway report with predicate devices for product code OGK
• Run a recall and safety report across every OGK manufacturer
• Watch product code OGK 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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