HCJClass II

Device, Skin Potential Measurement

21 CFR 882.1560 / Neurology

HCJ is the FDA product code for Device, Skin Potential Measurement, a class II device type, regulated under 21 CFR 882.1560. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1983-10-27, and no recalls.

Classification record

Product code: HCJ
Device name: Device, Skin Potential Measurement
Regulation: 21 CFR 882.1560
Device class: Class II
Review panel: Neurology
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 HCJ

By decision year

2 clearances under product code HCJ with a decision year between 1983 and 1983, 1983 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code HCJ by decision year
Year	Clearances
1983	2

Applicants with the most clearances

Product code HCJ

Applicants holding the most 510(k) clearances under product code HCJ
Applicant	Clearances
Share Int'L	1
Spelson Research Laboratories, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code HCJ

Recent recalls

Product code HCJ

FDA records show no recalls under product code HCJ.

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)