LYTENING 1— 510(k) K853832

Name: FDA 510(k) clearance K853832
Creator: U.S. Food and Drug Administration
Published: 1985-10-04

Substantially Equivalent

Amdev, Inc.

FDA 510(k) clearance K853832 for LYTENING 1, Substantially Equivalent on 1985-10-04. Applicant: Amdev, Inc.. Device class: 2.

Clearance details

Applicant: Amdev, Inc.
Product code: Code JGS
Device class: Class 2
Regulation: 21 CFR 862.1665
Advisory panel: Clinical Chemistry
Date received: 1985-09-13
Decision date: 1985-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haverhill, MA, US

Download summary PDF View on FDA.gov ↗

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K880917 — LYTENING 51988-05-27
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Adverse events under product code JGS

product code JGS

Malfunction: 535
Total: 535

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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