HJQClass I

Stereoscope, Ac-Powered

21 CFR 886.1870 / Ophthalmic

HJQ is the FDA product code for Stereoscope, Ac-Powered, a class I device type, regulated under 21 CFR 886.1870. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1983-03-24, and no recalls.

Classification record

Product code: HJQ
Device name: Stereoscope, Ac-Powered
Regulation: 21 CFR 886.1870
Device class: Class I
Review panel: Ophthalmic
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code HJQ

By decision year

1 clearance under product code HJQ with a decision year between 1983 and 1983, 1983 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code HJQ by decision year
Year	Clearances
1983	1

Applicants with the most clearances

Product code HJQ

Applicants holding the most 510(k) clearances under product code HJQ
Applicant	Clearances
Richard-Allan Medical Ind., Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code HJQ

K830625Class ICyto-StainRichard-Allan Medical Ind., Inc. / cleared 1983-03-24

Recent recalls

Product code HJQ

FDA records show no recalls under product code HJQ.

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)