OFM — Phlebotomy Blood Collection Kit Class II

FDA Device Classification

FDA product code OFM covers "Phlebotomy Blood Collection Kit", a Class II medical device regulated under 21 CFR 870.2750. Submissions are reviewed by the Cardiovascular panel.

Classification Details

Product Code
OFM
Device Class
Class II
Regulation Number
870.2750
Submission Type
Review Panel
HO
Medical Specialty
Cardiovascular
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.