NEQClass II

Device, Telemedicine, Robotic

21 CFR 876.1500 / Gastroenterology, Urology

NEQ is the FDA product code for Device, Telemedicine, Robotic, a class II device type, regulated under 21 CFR 876.1500. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 2001-12-10, and no recalls.

Classification record

Product code: NEQ
Device name: Device, Telemedicine, Robotic
Regulation: 21 CFR 876.1500
Device class: Class II
Review panel: Gastroenterology, Urology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code NEQ

By decision year

2 clearances under product code NEQ with a decision year between 2001 and 2001, 2001 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code NEQ by decision year
Year	Clearances
2001	2

Applicants with the most clearances

Product code NEQ

Applicants holding the most 510(k) clearances under product code NEQ
Applicant	Clearances
Computer Motion, Inc.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code NEQ

Recent recalls

Product code NEQ

FDA records show no recalls under product code NEQ.

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)