MODEL 2000 MONITOR— 510(k) K812828

Substantially Equivalent

Datascope Corp.

FDA 510(k) clearance K812828 for MODEL 2000 MONITOR, Substantially Equivalent on 1981-11-16. Applicant: Datascope Corp..

Clearance details

Applicant: Datascope Corp.
Product code: Code DRT
Advisory panel: Cardiovascular
Date received: 1981-10-08
Decision date: 1981-11-16
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.