ACCUTORR PLUS NON INVASIVE BLOOD PRESSURE MONITOR, MODEL # 0998-00-0117-XX— 510(k) K983575

Substantially Equivalent

Datascope Corp.

FDA 510(k) clearance K983575 for ACCUTORR PLUS NON INVASIVE BLOOD PRESSURE MONITOR, MODEL # 0998-00-0117-XX, Substantially Equivalent on 1999-05-13. Applicant: Datascope Corp..

Clearance details

Applicant: Datascope Corp.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1998-10-13
Decision date: 1999-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paramus, NJ, US

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Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.