JOTClass II

Electrode, Gel, Electrosurgical

21 CFR 878.4400 / General, Plastic Surgery

JOT is the FDA product code for Electrode, Gel, Electrosurgical, a class II device type, regulated under 21 CFR 878.4400. As of 2026-09-10, FDA records hold 9 510(k) clearances under this code, the most recent dated 1992-11-09, and no recalls.

Classification record

Product code: JOT
Device name: Electrode, Gel, Electrosurgical
Regulation: 21 CFR 878.4400
Device class: Class II
Review panel: General, Plastic Surgery
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 9
Ingested recalls: 0

Clearances, product code JOT

By decision year

9 clearances under product code JOT with a decision year between 1980 and 1992, 1987 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code JOT by decision year
Year	Clearances
1980	1
1987	2
1989	2
1990	1
1991	2
1992	1

Applicants with the most clearances

Product code JOT

Applicants holding the most 510(k) clearances under product code JOT
Applicant	Clearances
Amedic USA	1
Arbo Medical, Inc.	1
Echo Ultrasound	1
Geno Laboratories	1
H & P Industries, Inc.	1
Herbert Stanley Co.	1
R2 Corp.	1
Radionics, Inc.	1
Swedish Trade Council USA	1

Companies listing this code with FDA

Companies whose registered establishments list this code

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