EQLClass I

Laryngostroboscope

21 CFR 874.4750 / Ear, Nose, Throat

EQL is the FDA product code for Laryngostroboscope, a class I device type, regulated under 21 CFR 874.4750. As of 2026-09-10, FDA records hold 8 510(k) clearances under this code, the most recent dated 1999-03-17, and 2 recalls.

Classification record

Product code: EQL
Device name: Laryngostroboscope
Regulation: 21 CFR 874.4750
Device class: Class I
Review panel: Ear, Nose, Throat
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 8
Ingested recalls: 2

Clearances, product code EQL

By decision year

8 clearances under product code EQL with a decision year between 1977 and 1999, 1992 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code EQL by decision year
Year	Clearances
1977	1
1980	1
1982	1
1984	1
1989	1
1992	2
1999	1

Applicants with the most clearances

Product code EQL

Applicants holding the most 510(k) clearances under product code EQL
Applicant	Clearances
Kay Elemetrics Corp.	2
Bruel & Kjaer Industri A/S	1
JEDMED Instrument Company	1
Kelleher Corp.	1
Parke-Davis Co.	1
Pentax Precision Instrument Corp.	1
Richard Wolf Medical Instruments Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order