FDA product code OFP: Anesthesia Breathing Circuit Kit (Adult & Pediatric)

OFP is the FDA product code for anesthesia breathing circuit kit (adult & pediatric). It is a Class I device, regulated under 21 CFR 868.5240 and reviewed by the General Hospital panel. Devices under OFP reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. FDA has posted 33 recalls for OFP devices, 5 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 http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. 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 OFP devices

33 product recalls in 5 recall events; 5 initiated in the last five years and 5 still open. Most recent: 2025-03-12.

Frequently asked questions

What is FDA product code OFP?

OFP is the FDA product code for anesthesia breathing circuit kit (adult & pediatric). It is a Class I device, regulated under 21 CFR 868.5240 and reviewed by the General Hospital panel.

What device class is OFP?

Class I, regulation 21 CFR 868.5240. Typical premarket route: 510(k) exempt.

Have OFP devices been recalled?

Yes: 33 product recalls across 5 recall events; the most recent began 2025-03-12.

Next steps

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