KENL-ECG— 510(k) K811950

Name: FDA 510(k) clearance K811950
Creator: U.S. Food and Drug Administration
Published: 1981-08-13

Substantially Equivalent

Suzuken Co., Ltd.

FDA 510(k) clearance K811950 for KENL-ECG, Substantially Equivalent on 1981-08-13. Applicant: Suzuken Co., Ltd.. Device class: 2.

Clearance details

Applicant: Suzuken Co., Ltd.
Product code: Code DPS
Device class: Class 2
Regulation: 21 CFR 870.2340
Advisory panel: Cardiovascular
Date received: 1981-07-07
Decision date: 1981-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K870443 — KENZ-CARDICO 12011987-07-01

Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.