LRR
- Product code
- LRR
- Device name
- First Aid Kit With Drug
- Device class
- Class N
- Medical specialty
- Unknown
- Marketing pathway
- Enforcement Discretion
- 510(k) clearances (all years, FDA)
- 15 (all years; only the last 3 years are listed here)
FDA classification definition
Note: In addition to compliance with our convenience kit guidance, in regards to any drug products contained in this kit compliance with the Center for Drug Evaluation is required as well. www.fda.gov/cder/index.html - 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: LRR
Classification and pathway per current FDA publications. Data from openFDA (CC0).