JEGClass II

Analyzer, Gas, Argon, Gaseous-Phase

21 CFR 868.1075 / Anesthesiology

JEG is the FDA product code for Analyzer, Gas, Argon, Gaseous-Phase, a class II device type, regulated under 21 CFR 868.1075. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1988-05-16, and no recalls.

Classification record

Product code: JEG
Device name: Analyzer, Gas, Argon, Gaseous-Phase
Regulation: 21 CFR 868.1075
Device class: Class II
Review panel: Anesthesiology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code JEG

By decision year

1 clearance under product code JEG with a decision year between 1988 and 1988, 1988 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code JEG by decision year
Year	Clearances
1988	1

Applicants with the most clearances

Product code JEG

Applicants holding the most 510(k) clearances under product code JEG
Applicant	Clearances
Pro Care Laboratories, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code JEG

K880442Class IIBrushritePro Care Laboratories, Inc. / cleared 1988-05-16

Recent recalls

Product code JEG

FDA records show no recalls under product code JEG.

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)