POR

Parenteral Administration Kit

Product code

POR

Device name

Parenteral Administration Kit

Device class

Class 2

21 CFR

21 CFR 880.5440

Medical specialty

General Hospital

Marketing pathway

Enforcement Discretion

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 http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080216.htm . This kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market.

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