DXP — Transducer, Vessel Occlusion Class II

FDA Device Classification

FDA product code DXP covers "Transducer, Vessel Occlusion", a Class II medical device regulated under 21 CFR 870.2890. Submissions are reviewed by the Cardiovascular panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
DXP
Device Class
Class II
Regulation Number
870.2890
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K891180ingress technologiesTRANSESOPHAGEAL ULTRASOUND ACCESSORIES KITJune 15, 1989
K812639frontier productsUNICUFFOctober 2, 1981