OJG — Neurological Tray Class I

FDA Device Classification

FDA product code OJG covers "Neurological Tray", a Class I medical device regulated under 21 CFR 882.4525. Submissions are reviewed by the Neurology panel.

Classification Details

Product Code
OJG
Device Class
Class I
Regulation Number
882.4525
Submission Type
Review Panel
NE
Medical Specialty
Neurology
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.