FDA product code OHO: First Aid Kit Without Drug

OHO is the FDA product code for first aid kit without drug. It is a Class I device, regulated under 21 CFR 878.4014 and reviewed by the General and Plastic Surgery panel. Devices under OHO reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. FDA has posted 1 recall for OHO devices, 1 initiated in the last five years.

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

Recalls for OHO devices

1 product recalls in 1 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2026-07-07.

Frequently asked questions

What is FDA product code OHO?

OHO is the FDA product code for first aid kit without drug. It is a Class I device, regulated under 21 CFR 878.4014 and reviewed by the General and Plastic Surgery panel.

What device class is OHO?

Class I, regulation 21 CFR 878.4014. Typical premarket route: 510(k) exempt.

Have OHO devices been recalled?

Yes: 1 product recalls across 1 recall events; the most recent began 2026-07-07.

Next steps

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