TELEMETRY SOFTWARE FOR G-2000 ELECTROCARDIOGRAPH— 510(k) K850323

Name: FDA 510(k) clearance K850323
Creator: U.S. Food and Drug Administration
Published: 1985-05-16

Substantially Equivalent

Eaton Medical Group

FDA 510(k) clearance K850323 for TELEMETRY SOFTWARE FOR G-2000 ELECTROCARDIOGRAPH, Substantially Equivalent on 1985-05-16. Applicant: Eaton Medical Group. Device class: 2.

Clearance details

Applicant: Eaton Medical Group
Product code: Code DPS
Device class: Class 2
Regulation: 21 CFR 870.2340
Advisory panel: Cardiovascular
Date received: 1985-01-28
Decision date: 1985-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eaton, MI, US

Download summary PDF View on FDA.gov ↗

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K851627 — KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR1985-11-08
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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.