FDA product code LLQ: Cap, Cervical, Contraceptive
LLQ is the FDA product code for cap, cervical, contraceptive. It is a Class III device, reviewed by the Obstetrics and Gynecology panel. Devices under LLQ reach the market by PMA; FDA lists no cleared 510(k)s for it. 3 PMA applications cite this product code.
Classification
| Field | Value |
|---|---|
| Device name | Cap, Cervical, Contraceptive |
| Device class | Class III |
| Review panel | OB — Obstetrics and Gynecology |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for LLQ devices
openFDA lists no recalls for product code LLQ.
Frequently asked questions
What is FDA product code LLQ?
LLQ is the FDA product code for cap, cervical, contraceptive. It is a Class III device, reviewed by the Obstetrics and Gynecology panel.
What device class is LLQ?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code LLQ
- Run a recall and safety report across every LLQ manufacturer
- Watch product code LLQ 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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