LRQ
- Product code
- LRQ
- Device name
- Tracheostomy And Nasal Suctioning Kit
- Device class
- Class 1
- Medical specialty
- Unknown
- Marketing pathway
- Enforcement Discretion
- 510(k) clearances (all years, FDA)
- 6 (all years; only the last 3 years are listed here)
FDA classification 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.
Official FDA classification page: LRQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).