VITALNET(TM) SYSTEM (DINAMAP(TM), MODEL 2200)— 510(k) K871418

Substantially Equivalent

Critikon Company, LLC

FDA 510(k) clearance K871418 for VITALNET(TM) SYSTEM (DINAMAP(TM), MODEL 2200), Substantially Equivalent on 1987-07-29. Applicant: Critikon Company, LLC.

Clearance details

Applicant: Critikon Company, LLC
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1987-04-08
Decision date: 1987-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, 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.