OWL — Peripheral Catheter Insertion Kit Class II

FDA Device Classification

FDA product code OWL covers "Peripheral Catheter Insertion Kit", a Class II medical device regulated under 21 CFR 880.5200. Submissions are reviewed by the General Hospital panel.

Classification Details

Product Code
OWL
Device Class
Class II
Regulation Number
880.5200
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
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.