HS17/HS18 SERIES MONITORS— 510(k) K820670

Substantially Equivalent

Medtel Pty. , Ltd.

FDA 510(k) clearance K820670 for HS17/HS18 SERIES MONITORS, Substantially Equivalent on 1982-04-09. Applicant: Medtel Pty. , Ltd..

Clearance details

Applicant: Medtel Pty. , Ltd.
Product code: Code FLL
Advisory panel: General Hospital
Date received: 1982-03-11
Decision date: 1982-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FLL

product code FLL

Death: 3
Malfunction: 557
Total: 560

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.