ELECTROGLOTTOGRAPH— 510(k) K901609

Substantially Equivalent

Glottal Ent., Inc.

FDA 510(k) clearance K901609 for ELECTROGLOTTOGRAPH, Substantially Equivalent on 1990-06-28. Applicant: Glottal Ent., Inc.. Device class: 2.

Clearance details

Applicant: Glottal Ent., Inc.
Product code: Code KLX
Device class: Class 2
Regulation: 21 CFR 874.1325
Advisory panel: Ear, Nose, Throat
Date received: 1990-04-06
Decision date: 1990-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KLX

K990240 — ELECTROGLOTTOGRAPH1999-03-11
K841832 — GLOTTAL FREQUENCY ANALYSER1984-07-18
K821079 — ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG1982-05-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.