EGWClass II

Dryer, Film, Radiographic

21 CFR 892.1900 / Radiology

EGW is the FDA product code for Dryer, Film, Radiographic, a class II device type, regulated under 21 CFR 892.1900. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1990-07-13, and no recalls.

Classification record

Product code: EGW
Device name: Dryer, Film, Radiographic
Regulation: 21 CFR 892.1900
Device class: Class II
Review panel: Radiology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code EGW

By decision year

2 clearances under product code EGW with a decision year between 1977 and 1990, 1977 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code EGW by decision year
Year	Clearances
1977	1
1990	1

Applicants with the most clearances

Product code EGW

Applicants holding the most 510(k) clearances under product code EGW
Applicant	Clearances
G-C Intl. Corp.	1
Pako Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code EGW

Recent recalls

Product code EGW

FDA records show no recalls under product code EGW.

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)