EXWClass II

Pill, Radio

21 CFR 876.1725 / Gastroenterology, Urology

EXW is the FDA product code for Pill, Radio, a class II device type, regulated under 21 CFR 876.1725. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1984-06-28, and no recalls.

Classification record

Product code: EXW
Device name: Pill, Radio
Regulation: 21 CFR 876.1725
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: 1
Ingested recalls: 0

Clearances, product code EXW

By decision year

1 clearance under product code EXW with a decision year between 1984 and 1984, 1984 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code EXW by decision year
Year	Clearances
1984	1

Applicants with the most clearances

Product code EXW

Applicants holding the most 510(k) clearances under product code EXW
Applicant	Clearances
Oxford Medilog, 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 EXW.

Recent clearances

Product code EXW

K840934Class IIMedilog Ph1Oxford Medilog, Inc. / cleared 1984-06-28

Recent recalls

Product code EXW

FDA records show no recalls under product code EXW.

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)