MRP — Analyzer, Nitric Oxide Class II

FDA Device Classification

FDA product code MRP covers "Analyzer, Nitric Oxide", a Class II medical device regulated under 21 CFR 868.2380. Submissions are reviewed by the Anesthesiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MRP
Device Class
Class II
Regulation Number
868.2380
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K023014pulmonox medicalVIANOX DELIVERY SYSTEM, MODEL IAugust 14, 2003