OGI — Nasal Endotracheal Tube Holder Kit Class I

FDA Device Classification

FDA product code OGI covers "Nasal Endotracheal Tube Holder Kit", a Class I medical device regulated under 21 CFR 868.5770. Submissions are reviewed by the Anesthesiology panel.

Classification Details

Product Code
OGI
Device Class
Class I
Regulation Number
868.5770
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
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 www.Fda.Gov/cdrh/ode/convkit.Html. This kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market.