QDV — Iol Tray Class I

FDA Device Classification

FDA product code QDV covers "Iol Tray", a Class I medical device regulated under 21 CFR 886.4350. Submissions are reviewed by the Ophthalmic panel.

Classification Details

Product Code
QDV
Device Class
Class I
Regulation Number
886.4350
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

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.