PATIENT MONITOR 575— 510(k) K830433

Substantially Equivalent

Kone Instruments, Inc.

FDA 510(k) clearance K830433 for PATIENT MONITOR 575, Substantially Equivalent on 1983-03-24. Applicant: Kone Instruments, Inc..

Clearance details

Applicant: Kone Instruments, Inc.
Product code: Code DRT
Advisory panel: Cardiovascular
Date received: 1983-02-09
Decision date: 1983-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DRT

product code DRT

Death: 4
Total: 4

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.