DXPClass II

Transducer, Vessel Occlusion

21 CFR 870.2890 / Cardiovascular

DXP is the FDA product code for Transducer, Vessel Occlusion, a class II device type, regulated under 21 CFR 870.2890. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1989-06-15, and no recalls.

Classification record

Product code: DXP
Device name: Transducer, Vessel Occlusion
Regulation: 21 CFR 870.2890
Device class: Class II
Review panel: Cardiovascular
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code DXP

By decision year

2 clearances under product code DXP with a decision year between 1981 and 1989, 1981 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code DXP by decision year
Year	Clearances
1981	1
1989	1

Applicants with the most clearances

Product code DXP

Applicants holding the most 510(k) clearances under product code DXP
Applicant	Clearances
Frontier Products	1
Ingress Technologies, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code DXP.

Recent clearances

Product code DXP

Recent recalls

Product code DXP

FDA records show no recalls under product code DXP.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)