LRO

General Surgery Tray

Product code
LRO
Device name
General Surgery Tray
Device class
Class 2
21 CFR
21 CFR 878.4370
Medical specialty
General, Plastic Surgery
Marketing pathway
Enforcement Discretion
510(k) clearances (last 3 years)
110

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

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: LRO
Classification and pathway per current FDA publications. Data from openFDA (CC0).