OFZ — Blood Specimen Collection Kit (Excludes Hiv Testing) Class I

FDA Device Classification

FDA product code OFZ covers "Blood Specimen Collection Kit (Excludes Hiv Testing)", a Class I medical device regulated under 21 CFR 868.1100. Submissions are reviewed by the Anesthesiology panel.

Classification Details

Product Code
OFZ
Device Class
Class I
Regulation Number
868.1100
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 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.